Butalbital, Aspirin, and Caffeine Tablets, USP CIII Rev. 04/03 Rx Only

Manufacturer
Rebel Distributors Corp
Effective date
2010-12-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:10:50

Label at a glance#

ProductButalbital, Aspirin and Caffeine
Active ingredientBUTALBITAL, ASPIRIN, CAFFEINE
Label structure11 sections

Indications and uses

Butalbital, Aspirin and Caffeine Tablets are indicated for the relief of the symptom complex of tension (or muscle contraction) headache.

Dosage and administration

Oral: One or two tablets every four hours as needed. Do not exceed 6 tablets per day. Medication should be taken with food or a full glass of water or milk to lessen gastric irritation caused by aspirin.

Label contents#

Full prescribing information#

DESCRIPTION:

DESCRIPTION SECTION

Each Butalbital, Aspirin, and Caffeine Tablet for oral administration contains:

Butalbital, USP.....................50 mg

Aspirin, USP.......................325 mg

Caffeine, USP.......................40 mg

Butalbital, 5-allyl-5-isobutylbarbituric acid, a white, odorless, crystalline powder having a slightly bitter taste, is a short to intermediate-acting barbiturate. It has the following structural formula:

Structural formula for Butalbital
Structural formula for Butalbital

C11H16N2O3 M.W. 224.26

Aspirin, salicylic acid acetate, is a non-opiate analgesic, anti-inflammatory and antipyretic agent. It occurs as a white, crystalline tabular or needle-like powder and is odorless or has a faint odor. It has the following structural formula:

Structural formula for Aspirin
Structural formula for Aspirin

C9H8O4 M.W. 180.16

Caffeine, 1,3,7,-trimethylxanthine, is a central nervous system stimulant which occurs as a white powder or white glistening needles. It also has a bitter taste. Its structure is as follows:

Structural formula for Caffeine
Structural formula for Caffeine

C8H10N4O2 M.W. 194.19

Inactive Ingredients: Corn Starch, Hydrogenated Vegetable Oil, Microcrystalline Cellulose, Pregelatinized Starch, Sodium Starch Glycolate and Talc.

CLINICAL PHARMACOLOGY:

CLINICAL PHARMACOLOGY SECTION

Pharmacologically, Butalbital, Aspirin, and Caffeine Tablets combine the analgesic properties of aspirin with the anxiolytic and muscle relaxant properties of butalbital.

The clinical effectiveness of a product containing butalbital, aspirin, and caffeine in tension headache has been established in double-blind, placebo-controlled, multiclinic trials. A factorial design study compared the combination product with each of its major components. This study demonstrated that each component contributes to the efficacy of the combination product in the treatment of the target symptoms of tension headache (headache pain, psychic tension, and muscle contraction in the head, neck, and shoulder region). For each symptom and the symptom complex as a whole, the product containing butalbital, aspirin, and caffeine was shown to have significantly superior clinical effects to either of the major components alone.

INDICATIONS AND USAGE:

INDICATIONS & USAGE SECTION

Butalbital, Aspirin and Caffeine Tablets are indicated for the relief of the symptom complex of tension (or muscle contraction) headache.

CONTRAINDICATIONS:

CONTRAINDICATIONS SECTION

Hypersensitivity to aspirin, caffeine or barbiturates. Patients with porphyria.

PRECAUTIONS:

PRECAUTIONS SECTION

1. General:

GENERAL PRECAUTIONS SECTION

Butalbital, Aspirin, and Caffeine Tablets should be used with caution in patients with certain medical problems, including those with a history of asthma, allergies and nasal polyps. Also, the drug must be prescribed carefully for patients with hemophilia or other bleeding problems, peptic ulcer, renal impairment, or a history of drug abuse or dependence.

2. Information for Patients:

INFORMATION FOR PATIENTS SECTION

Butalbital, Aspirin, and Caffeine Tablets may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks, such as driving a car or operating machinery. The patient should be cautioned accordingly.

3. Drug Interactions:

DRUG INTERACTIONS SECTION

Patients receiving narcotic analgesics, antipsychotics, antianxiety agents, or other CNS depressants (including alcohol) concomitantly with Butalbital, Aspirin, and Caffeine Tablets may exhibit additive CNS depressant effects. When combined therapy is contemplated, the dose of one or both agents should be reduced.

DRUGSEFFECT
Aspirin w/anti-inflammatory agents

Increased
ulcerogenic effects.

Butalbital w/coumarin anticoagulants

Decreased effect of
anticoagulant
because of
increased
metabolism
resulting from
enzyme induction.

Butalbital w/tricyclic antidepressants

Decreased blood
levels of the
antidepressant.

4. Usage in Pregnancy:

PREGNANCY SECTION

Adequate studies have not been performed in animals to determine whether this drug affects fertility in males or females, has teratogenic potential or has other adverse effects on the fetus. While there are no well-controlled studies in pregnant women, over twenty years of marketing and clinical experience does not include any positive evidence of adverse effects on the fetus. Although there is no clearly defined risk, such experience cannot exclude the possibility of infrequent or subtle damage to the human fetus. Butalbital, Aspirin, and Caffeine Tablets should be used in pregnant women only when clearly needed.

5. Nursing Mothers:

NURSING MOTHERS SECTION

The effects of Butalbital, Aspirin, and Caffeine Tablets on infants of nursing mothers are not known. Salicylates and barbiturates are excreted in the breast milk of nursing mothers. The serum levels in infants are believed to be insignificant with therapeutic doses.

6. Pediatric Use:

PEDIATRIC USE SECTION

Safety and effectiveness in children below the age of 12 have not been established.

ADVERSE REACTIONS:

ADVERSE REACTIONS SECTION

The most frequent adverse reactions are drowsiness and dizziness. Less frequent adverse reactions are lightheadedness and gastrointestinal disturbances including nausea, vomiting, and flatulence. Mental confusion or depression can occur due to intolerance or overdosage of butalbital.

Several cases of dermatological reactions including toxic epidermal necrolysis and erythema multiforme have been reported.

DRUG ABUSE AND DEPENDENCE:

DRUG ABUSE AND DEPENDENCE SECTION

Butalbital, Aspirin, and Caffeine Tablets are classified as a Schedule III controlled substance.

Prolonged use of barbiturates can produce drug dependence, characterized by psychic dependence, and less frequently, physical dependence and tolerance. The abuse liability of Butalbital, Aspirin, and Caffeine Tablets are similar to that of other barbiturate-containing drug combinations. Caution should be exercised when prescribing medication for patients with a known propensity for taking excessive quantities of drugs, which is not uncommon in patients with chronic tension headache.

OVERDOSAGE:

OVERDOSAGE SECTION

Symptoms: The toxic effects of acute overdosage of Butalbital, Aspirin, and Caffeine Tablets are attributable mainly to its barbiturate component, and, to a lesser extent, aspirin. Because toxic effects of caffeine occur in very high dosages only, the possibility of significant caffeine toxicity from Butalbital, Aspirin, and Caffeine Tablet overdosage in unlikely. Symptoms attributable to acute barbiturate poisoning include drowsiness, confusion, and coma; respiratory depression; hypotension; shock. Symptoms attributable to acute aspirin poisoning include hyperpnea; acid-base disturbances with development of metabolic acidosis; vomiting and abdominal pain; tinnitus; hyperthermia; hypoprothrombinemia; restlessness; delirium; convulsions. Acute caffeine poisoning may cause insomnia, restlessness, tremor, and delirium; tachycardia and extrasystoles.

Treatment: Treatment consists primarily of management of barbiturate intoxication and the correction of the acid-base imbalance due to salicylism. Vomiting should be induced mechanically or with emetics in the conscious patient. Gastric lavage may be used if the pharyngeal and laryngeal reflexes are present and if less than four hours have elapsed since ingestion. A cuffed endotracheal tube should be inserted before gastric lavage of the unconscious patient and when necessary to provide assisted respiration. Diuresis, alkalinization of the urine, and correction of electrolyte disturbances should be accomplished through administration of intravenous fluids such as 1% sodium bicarbonate in 5% dextrose injection. Meticulous attention should be given to maintaining adequate pulmonary ventilation. Correction of hypotension may require the administration of norepinephrine bitartrate of phenylephrine hydrochloride by intravenous infusion. In severe cases of intoxication, peritoneal dialysis, hemodialysis, or exchange transfusion may be lifesaving. Hypoprothrombinemia should be treated with Vitamin K, intravenously.

DOSAGE AND ADMINISTRATION:

DOSAGE & ADMINISTRATION SECTION

Oral: One or two tablets every four hours as needed. Do not exceed 6 tablets per day.

Medication should be taken with food or a full glass of water or milk to lessen gastric irritation caused by aspirin.

HOW SUPPLIED:

HOW SUPPLIED SECTION

Butalbital, Aspirin and Caffeine Tablets, USP 50 mg/325 mg/40 mg: White, round, unscored tablets; imprinted “West-ward 785”.

Bottles of 60 tablets, NDC 21695-354-60.

Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature]. Protect from light and moisture.

Dispense in a tight, light-resistant container as defined in the USP using a child-resistant closure.

Manufactured By:
West-ward Pharmaceutical Corp.
Eatontown, NJ 07724
Revised April 2003

Repackaged by:

Rebel Distributors Corp

Thousand Oaks, CA 91320

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Butalb/ASA/Caffeine 50/325/40mg
Butalb/ASA/Caffeine 50/325/40mg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
238135butalbital 50 MG / aspirin 325 MG / caffeine 40 MG Oral TabletPSN1
238135aspirin 325 MG / butalbital 50 MG / caffeine 40 MG Oral TabletSCD1
238135ASA 325 MG / butalbital 50 MG / caffeine 40 MG Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASPIRIN Pharmacologic Class Indexing3Indexing - Pharmacologic Class20191108
BUTALBITAL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
11939cf5-0ea7-5df5-5127-00a7ce07fd7fProduct name520250115
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
88300afc-e1c4-ad17-c80b-4957f1b809a5Product name520250113
79e1734e-f721-4d46-978a-be382f771672Product name220230110
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
d7724692-1155-4cc8-a415-22f5fc4aec35Product name620220216
bde672ba-4805-28d0-1986-73543d41b412Product name220210201
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
103b151b-b17f-42ac-8624-3ef62f5e2975Product name220200507
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
ade821ba-260a-47e2-bd89-743e27ac9906Product name120161121
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
9425d234-4ae1-4b53-adc6-8cc7af6dd657Product name120150929
2a21311a-89e2-0e83-2ebd-117f9798b2b2Product name120140508
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
3ed6b849-48b8-8899-c288-6eeb396123b6Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
9007e8a7-ff50-f9b9-7945-f2a1deadd94eProduct name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21695-354-602019-09-24C16284748780-1934fe258-489c-48b1-e053-8cdaa90a720aButalbital, Aspirin, and Caffeine Tablets, USP CIII Rev. 04/03 Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-354-60Butalbital, Aspirin and Caffeine60 in 1 BOTTLETABLET601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-354BUTALBITAL, ASPIRIN AND CAFFEINE TABLET [REBEL DISTRIBUTORS CORP]1Legacy NDC, 1 package rows20101220_4e10129b-41a3-4572-9564-6f8366b627dc.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-354-60EA - Each21695-354f3acf897-817e-4710-ac5a-d16d6279d0e712012-07-24
0143-1785-01EA - Each0143-178566237812-01e7-4407-bc62-cfb56482860612012-07-24
0143-1785-10EA - Each0143-1785fb1ecd62-7bab-44cc-875b-7bea0b08417012012-07-24
0143-1785-30EA - Each0143-1785dbbb0671-2494-4b13-aa7d-9add99f52cc512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76E1
BUTALBITALACTIVE INGREDIENTKHS0AZ4JVK1
CAFFEINEACTIVE INGREDIENT3G6A5W338E1
ASPIRINACTIVE MOIETYR16CO5Y76E1
BUTALBITALACTIVE MOIETYKHS0AZ4JVK1
CAFFEINEACTIVE MOIETY3G6A5W338E1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJ1
TALCINACTIVE INGREDIENT7SEV7J4R1U1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21695-35421695-354-60
0143-1785

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 85 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
TALCTALC7SEV7J4R1UTABLET, FOR SUSPENSION / ORAL24 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE, DELAYED RELEASE / ORAL216 mgExact identifier — unii candidate
22 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, COATED / ORAL256 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UCAPSULE, EXTENDED RELEASE / ORAL5119 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UGRANULE, DELAYED RELEASE / ORAL525 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UCAPSULE, COATED, EXTENDED RELEASE / ORAL20 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCONCENTRATE / ORALNAExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UGRANULE / ORAL322 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL357 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UPOWDER, FOR SUSPENSION / ORAL735 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, ORALLY DISINTEGRATING / ORAL100 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UELIXIR / ORAL4.5 mg/5mlExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, FILM COATED / ORAL91 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, DELAYED RELEASE / ORAL349 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJDROPS / ORALNAExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTROCHE / ORAL300 mgExact identifier — unii candidate
28 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET / ORAL1116 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UPELLET / ORAL69 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UOINTMENT / TOPICAL74.6 %w/wExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UPOWDER / TOPICAL9235 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61USUSPENSION / ORAL1600 mgExact identifier — unii candidate
28 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / SUBLINGUAL43.2 mgExact identifier — unii candidate
28 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJPASTILLE / ORALNAExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, DELAYED RELEASE PARTICLES / ORAL56 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, CHEWABLE / ORAL180 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, EXTENDED RELEASE / ORAL300 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJSUSPENSION, EXTENDED RELEASE / ORAL113 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, DELAYED RELEASE PARTICLES / ORAL580 mgExact identifier — unii candidate
28 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UPOWDER, FOR SOLUTION / ORAL690 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, ORALLY DISINTEGRATING / ORAL80 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FOR SUSPENSION / ORAL20100 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, SUGAR COATED / ORALNAExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1ULOZENGE / ORAL50 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UGRANULE, FOR SUSPENSION / ORAL296 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE, EXTENDED RELEASE / ORAL194 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, COATED / ORAL920 mgExact identifier — unii candidate
28 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE, COATED, EXTENDED RELEASE / ORAL19 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, CHEWABLE / ORAL202 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61USUSPENSION, EXTENDED RELEASE / ORAL1120 mgExact identifier — unii candidate
28 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / ORAL6184 mgExact identifier — unii candidate
28 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL1576 mgExact identifier — unii candidate
28 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, ORALLY DISINTEGRATING, DELAYED RELEASE / ORAL21 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, CHEWABLE / ORAL1725 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UGUM, CHEWING / BUCCALNAExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE / ORAL5785 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UPELLET / ORAL1140 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, FILM COATED, EXTENDED RELEASE / ORAL60 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET / SUBLINGUAL32.4 mgExact identifier — unii candidate
35 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, CHEWABLE, EXTENDED RELEASE / ORAL18 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, EXTENDED RELEASE / ORAL5119 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UCAPSULE, DELAYED RELEASE / ORAL420 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UGRANULE, FOR SUSPENSION / ORAL278 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1UCAPSULE / ORAL729 mgExact identifier — unii candidate
35 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJINSERT / VAGINAL147 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UGRANULE, DELAYED RELEASE / ORAL789.6 mgExact identifier — unii candidate
28 equally ranked IID candidates
TALCTALC7SEV7J4R1USUSPENSION, EXTENDED RELEASE / ORAL46 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED, EXTENDED RELEASE / ORAL615 mgExact identifier — unii candidate
28 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, EXTENDED RELEASE / ORAL184 mgExact identifier — unii candidate
22 equally ranked IID candidates
TALCTALC7SEV7J4R1USUSPENSION / ORAL234 mgExact identifier — unii candidate
35 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET / BUCCAL18 mgExact identifier — unii candidate
28 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A086162-002BUTALBITAL, ASPIRIN AND CAFFEINEASPIRIN; BUTALBITAL; CAFFEINE325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1984-02-16

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1984-02-1684e616aacf4f…
2026-08-18 06:07:402026-07A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1984-02-16caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**TABLET / ORALRLD1984-02-16011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-1631067a03dcf5…
2025-08-23 18:47 UTC2025-08A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-166a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-1603ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-162680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-165bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-1679d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-161e350fbaab3a…
2024-05-31 18:47 UTC2024-05A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-168072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-165c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-165d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-164b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALAARS1984-02-1674a2ff9319b5…
2022-03-09 01:35 UTC2022-03A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-16bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-16782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-1687673890dc5c…
2021-03-12 10:30 UTC2021-03A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-165aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-168869cabd3fbd…
2020-11-12 02:37 UTC2020-11A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORAL1984-02-16c0c555d07b60…
2019-12-14 00:12 UTC2019-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALAARS1984-02-163f01610625f2…
2019-09-15 20:21 UTC2019-09A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALAARS1984-02-16b00525d2431f…
2019-07-19 19:46 UTC2019-07A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALAARS1984-02-16ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-166a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-161c564ffb4f44…
2023-12-20 04:57 UTC2023-12A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-169b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-163f0d92c62455…
2023-05-13 08:27 UTC2023-05A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16053a50430f4f…
2023-01-26 05:58 UTC2023-01A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-163bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-163a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A086162-002BUTALBITAL, ASPIRIN AND CAFFEINE325MG;50MG;40MGTABLET / ORALRLD1984-02-16f41ea6bd6efb…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2019-12-13 00:20 UTC2019-12A086162-002AA174a2ff9319b5…
2019-12-14 00:12 UTC2019-12A086162-002AA13f01610625f2…
2019-09-15 20:21 UTC2019-09A086162-002AA1b00525d2431f…
2019-07-19 19:46 UTC2019-07A086162-002AA1ea99ee380514…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4e10129b-41a3-4572-9564-6f8366b627dc4e10129b-41a3-4572-9564-6f8366b627dc2010-12-10Adverse reactionsExact identifier
spl id: 4e10129b-41a3-4572-9564-6f8366b627dc
spl set id: 4e10129b-41a3-4572-9564-6f8366b627dc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.