Orphenadrine Citrate, Aspirin and Caffeine Tablets

Manufacturer
Rebel Distributors Corp
Effective date
2010-10-22
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:10:34

Label at a glance#

ProductOrphenadrine Citrate, Aspirin and Caffeine
Active ingredientORPHENADRINE CITRATE, ASPIRIN, CAFFEINE
Label structure11 sections

Indications and uses

Symptomatic relief of mild to moderate pain of acute musculoskeletal disorders. The orphenadrine component is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions. The mode of action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. Orphenadrine Citrate, Aspirin, and...

Dosage and administration

Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 25 mg/385 mg/30 mg: Adults 1 to 2 tablets 3 to 4 times daily. Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 50 mg/770 mg/60 mg: Adults 1/2 to 1 tablet 3 to 4 times daily.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Each tablet, for oral administration, contains Orphenadrine Citrate USP, 25 mg or 50 mg, Aspirin USP, 385 mg or 770 mg, Caffeine USP, 30 mg or 60 mg.

Orphenadrine citrate, N, N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethylamine citrate (1:1), is a centrally acting (brain stem) compound. It occurs as a white, practically odorless, crystalline powder, having a bitter taste. Its molecular formula is C18H23NO.C6H8O7 with a molecular weight of 461.51. The structural formula is shown below.

Orphenadrine Citrate Chemical Structure
Orphenadrine Citrate Chemical Structure

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. Its molecular formula is C9H8O4, with a molecular weight of 180.16. The structural formula is shown below.

Aspirin Chemical Structure
Aspirin Chemical Structure

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 molecular formula is C8H1 0N4O2, with a molecular weight of 194.19. The structural formula is shown below.

Caffeine Chemical Structure
Caffeine Chemical Structure

Each tablet contains the following inactive ingredients: colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C Blue No. 1, FD&C Yellow No. 10, anhydrous lactose, microcrystalline cellulose, povidone, pregelatinized starch, stearic acid, and sodium lauryl sulfate.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Orphenadrine citrate is a centrally acting (brain stem) compound which in animals selectively blocks facilitatory functions of the reticular formulation. Orphenadrine does not produce myoneural block, nor does it affect crossed extensor reflexes. Orphenadrine prevents nicotine-induced convulsions but not those produced by strychnine.

Chronic administration of Orphenadrine Citrate, Aspirin, and Caffeine to dogs and rats has revealed no drug-related toxicity. No blood or urine changes were observed, nor were there any macroscopic or microscopic pathological changes detected. Extensive experience with combinations containing aspirin and caffeine has established them as safe agents. The addition of orphenadrine citrate does not alter the toxicity of aspirin and caffeine.

The mode of therapeutic action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. Orphenadrine citrate also possesses anticholinergic actions.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

  1. Symptomatic relief of mild to moderate pain of acute musculoskeletal disorders.
  2. The orphenadrine component is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions.

    The mode of action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. Orphenadrine Citrate, Aspirin, and Caffeine Tablets do not directly relax tense skeletal muscles in man.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Because of the mild anti-cholinergic effect of orphenadrine, Orphenadrine Citrate, Aspirin, and Caffeine Tablets should not be used in patients with glaucoma, pyloric or duodenal obstruction, achalasia, prostatic hypertrophy, or obstructions at the bladder neck. Orphenadrine Citrate, Aspirin, and Caffeine Tablets are also contraindicated in patients with myasthenia gravis and in patients known to be sensitive to aspirin or caffeine.

The drug is contraindicated in patients who have demonstrated a previous hypersensitivity to the drug.

WARNINGS

WARNINGS SECTION

Reye’s Syndrome may develop in individuals who have chicken pox, influenza, or flu symptoms. Some studies suggest possible association between the development of Reye’s Syndrome and the use of medicines containing salicylate or aspirin. Orphenadrine Citrate, Aspirin, and Caffeine Tablets contain aspirin and therefore are not recommended for use in patients with chicken pox, influenza, or flu symptoms. Orphenadrine Citrate, Aspirin, and Caffeine Tablets may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or driving a motor vehicle: ambulatory patients should therefore be cautioned accordingly.

Aspirin should be used with extreme caution in the presence of peptic ulcers and coagulation abnormalities.

Usage in Pregnancy

SPL UNCLASSIFIED SECTION

Since safety of the use of this preparation in pregnancy, during lactation, or in the child-bearing age has not been established, use of the drug in such patients requires that the potential benefits of the drug be weighed against its possible hazard to the mother and child.

Usage in Children

SPL UNCLASSIFIED SECTION

The safe and effective use of this drug in children has not been established. Usage of this drug in children under 12 years of age is not recommended.

PRECAUTIONS

PRECAUTIONS SECTION

Confusion, anxiety and tremors have been reported in a few patients receiving propoxyphene and orphenadrine concomitantly. As these symptoms may be simply due to an additive effect, reduction of dosage and/or discontinuation of one or both agents is recommended in such cases.

Safety of continuous long term therapy with Orphenadrine Citrate, Aspirin, and Caffeine Tablets has not been established; therefore, if Orphenadrine Citrate, Aspirin, and Caffeine Tablets are prescribed for prolonged use, periodic monitoring of blood, urine and liver function values is recommended.

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Side effects of Orphenadrine Citrate, Aspirin, and Caffeine Tablets are those seen with aspirin and caffeine or those usually associated with mild anticholinergic agents. These may include tachycardia, palpitation, urinary hesitancy or retention, dry mouth, blurred vision, dilation of the pupil, increased intraocular tension, weakness, nausea, vomiting, headache, dizziness, constipation, drowsiness, and rarely, urticaria and other dermatoses. Infrequently, an elderly patient may experience some degree of confusion. Mild central excitation and occasional hallucinations may be observed. These mild side effects can usually be eliminated by reduction in dosage. One case of aplastic anemia associated with the use of Orphenadrine Citrate, Aspirin, and Caffeine Tablets has been reported. No causal relationship has been established. Rare G.I. hemorrhage due to aspirin content may be associated with the administration of Orphenadrine Citrate, Aspirin, and Caffeine Tablets. Some patients may experience transient episodes of lightheadedness, dizziness or syncope.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 25 mg/385 mg/30 mg: Adults 1 to 2 tablets 3 to 4 times daily.

Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 50 mg/770 mg/60 mg: Adults 1/2 to 1 tablet 3 to 4 times daily.

HOW SUPPLIED

HOW SUPPLIED SECTION

Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 50 mg/770 mg/60 mg are scored, capsule-shaped, layered tablets colored white and green, imprinted SZ 491 and are supplied as:

NDC 21695-726-30 bottles of 30

NDC 21695-726-45 bottles of 45

Storage

STORAGE AND HANDLING SECTION

Store at 20°-25°C (68°-77° F) (see USP Controlled Room Temperature).

Protect from moisture.

SPL UNCLASSIFIED SECTION

Sandoz Inc.

Princeton, NJ 08540

Repackaged by:

Rebel Distributors Corp

Thousand Oaks, CA 91320


50 mg/770 mg/60 mg Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Orphenadrine

Citrate, Aspirin,

and Caffeine

Tablets

50 mg/770 mg/60 mg

Rx only

Orphenadrine/Aspirin/Caffeine 50/770/60mg
Orphenadrine/Aspirin/Caffeine 50/770/60mg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
994535orphenadrine citrate 50 MG / aspirin 770 MG / caffeine 60 MG Oral TabletPSN1
994535aspirin 770 MG / caffeine 60 MG / orphenadrine citrate 50 MG Oral TabletSCD1
994535ASA 770 MG / caffeine 60 MG / orphenadrine citrate 50 MG Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ASPIRIN Pharmacologic Class Indexing3Indexing - Pharmacologic Class20191108
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
ORPHENADRINE 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
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
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
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
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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-726-30Orphenadrine Citrate, Aspirin and Caffeine30 in 1 BOTTLETABLET, MULTILAYER301
21695-726-45Orphenadrine Citrate, Aspirin and Caffeine45 in 1 BOTTLETABLET, MULTILAYER451

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-726ORPHENADRINE CITRATE, ASPIRIN AND CAFFEINE TABLET, MULTILAYER [REBEL DISTRIBUTORS CORP]1Legacy NDC, 2 package rows20101124_8e41b33e-f71f-4a5e-b88f-cdfefb2bee20.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-726-30EA - Each21695-726c8b05896-1dc2-4276-b0e2-7ce72cfeeaef12012-07-24
21695-726-45EA - Each21695-726aae3a7b1-8576-4c02-9493-d61459d4dbf112012-07-24
0185-0714-01EA - Each0185-07148237ee60-d066-4e60-a05d-216f4aba5d2612012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76E1
CAFFEINEACTIVE INGREDIENT3G6A5W338E1
ORPHENADRINE CITRATEACTIVE INGREDIENTX0A40N8I4S1
ASPIRINACTIVE MOIETYR16CO5Y76E1
CAFFEINEACTIVE MOIETY3G6A5W338E1
ORPHENADRINEACTIVE MOIETYAL805O9OG91
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMK1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH481
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3G1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBD1
POVIDONEINACTIVE INGREDIENTFZ989GH94E1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU41
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141J1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJ1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65AP1

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
21695-72621695-726-30, 21695-726-45
0185-0714

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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 6 · 308 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / VAGINAL12 mgExact identifier — unii candidate
42 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JSUSPENSION, EXTENDED RELEASE / ORAL0.08 mg/1mlExact identifier — unii candidate
42 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4GRANULE, FOR SUSPENSION, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
49 equally ranked IID candidates
D&C YELLOW NO. 10D&C YELLOW NO. 1035SW5USQ3GTABLET, CHEWABLE / ORAL4 mgExact identifier — unii candidate
31 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APTABLET / ORAL336 mgExact identifier — unii candidate
26 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4CAPSULE / ORAL300 mgExact identifier — unii candidate
49 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDPASTE, DENTIFRICE / DENTALNAExact identifier — unii candidate
37 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, ORALLY DISINTEGRATING / ORAL100 mgExact identifier — unii candidate
22 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94EFILM, EXTENDED RELEASE / TRANSDERMALNAExact identifier — unii candidate
30 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJDROPS / ORALNAExact identifier — unii candidate
22 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, ORALLY DISINTEGRATING / ORAL16 mgExact identifier — unii candidate
42 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4CAPSULE / RESPIRATORY (INHALATION)NAExact identifier — unii candidate
49 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APTABLET / BUCCAL6 mgExact identifier — unii candidate
26 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDTABLET, COATED / ORAL0.52 mgExact identifier — unii candidate
37 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94ECAPSULE, COATED, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
30 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48INJECTION / INTRAMUSCULAR1 %w/vExact identifier — unii candidate
22 equally ranked IID candidates
D&C YELLOW NO. 10D&C YELLOW NO. 1035SW5USQ3GCAPSULE / ORAL20 mgExact identifier — unii candidate
31 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE / ORAL5785 mgExact identifier — unii candidate
22 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJSUSPENSION, EXTENDED RELEASE / ORAL113 mgExact identifier — unii candidate
22 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDCONCENTRATE / BUCCALNAExact identifier — unii candidate
37 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDCAPSULE, EXTENDED RELEASE / ORAL1 mgExact identifier — unii candidate
37 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDSUSPENSION / ORAL1 mgExact identifier — unii candidate
37 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, EXTENDED RELEASE / ORAL184 mgExact identifier — unii candidate
22 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48GRANULE, FOR SUSPENSION / ORAL282 mgExact identifier — unii candidate
22 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APAEROSOL, FOAM / TOPICAL8 %w/wExact identifier — unii candidate
26 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4CAPSULE, COATED / ORAL3 mgExact identifier — unii candidate
49 equally ranked IID candidates
ANHYDROUS LACTOSEANHYDROUS LACTOSE3SY5LH9PMKTABLET / SUBLINGUAL128 mgExact identifier — unii candidate
21 equally ranked IID candidates
ANHYDROUS LACTOSEANHYDROUS LACTOSE3SY5LH9PMKTABLET, FOR SUSPENSION / ORAL15 mgExact identifier — unii candidate
21 equally ranked IID candidates
D&C YELLOW NO. 10D&C YELLOW NO. 1035SW5USQ3GGUM, CHEWING / ORAL2 mgExact identifier — unii candidate
31 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4FILM, EXTENDED RELEASE / TRANSDERMAL49 mgExact identifier — unii candidate
49 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, COATED / ORAL176 mgExact identifier — unii candidate
49 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94ECAPSULE, DELAYED RELEASE PELLETS / ORAL32 mgExact identifier — unii candidate
30 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDTABLET / ORAL27.53 mgExact identifier — unii candidate
37 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UPOWDER, FOR SOLUTION / ORAL690 mgExact identifier — unii candidate
28 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDSYRUP / ORAL0.05 mg/5mlExact identifier — unii candidate
37 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCREAM / TOPICAL214 mgExact identifier — unii candidate
42 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UCAPSULE, DELAYED RELEASE / ORAL366 mgExact identifier — unii candidate
28 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94ETABLET, FILM COATED, EXTENDED RELEASE / ORAL17 mgExact identifier — unii candidate
30 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCAPSULE, COATED PELLETS / ORAL1 mgExact identifier — unii candidate
42 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48TABLET, CHEWABLE / ORAL216 mgExact identifier — unii candidate
22 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJCAPSULE, EXTENDED RELEASE / ORAL194 mgExact identifier — unii candidate
22 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94ECAPSULE / ORAL300 mgExact identifier — unii candidate
30 equally ranked IID candidates
CROSCARMELLOSE SODIUMCROSCARMELLOSE SODIUMM28OL1HH48GRANULE / ORAL150 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED, EXTENDED RELEASE / ORAL615 mgExact identifier — unii candidate
28 equally ranked IID candidates
STEARIC ACIDSTEARIC ACID4ELV7Z65APSOAP / TOPICAL6 %w/wExact identifier — unii candidate
26 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJINSERT / VAGINAL147 mgExact identifier — unii candidate
22 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, EXTENDED RELEASE / ORAL5119 mgExact identifier — unii candidate
28 equally ranked IID candidates
FD&C BLUE NO. 1FD&C BLUE NO. 1H3R47K3TBDFILM, SOLUBLE / ORAL0.04 mgExact identifier — unii candidate
37 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UCAPSULE, COATED PELLETS / ORAL456 mgExact identifier — unii candidate
28 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, EXTENDED RELEASE / ORAL320 mgExact identifier — unii candidate
42 equally ranked IID candidates
D&C YELLOW NO. 10D&C YELLOW NO. 1035SW5USQ3GCAPSULE, COATED PELLETS / ORAL0.01 mgExact identifier — unii candidate
31 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, ORALLY DISINTEGRATING / ORAL68 mgExact identifier — unii candidate
49 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UGRANULE, DELAYED RELEASE / ORAL789.6 mgExact identifier — unii candidate
28 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TAMPON / VAGINALNAExact identifier — unii candidate
49 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JCAPSULE, DELAYED RELEASE PELLETS / ORAL99 mgExact identifier — unii candidate
42 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4TABLET, FILM COATED, EXTENDED RELEASE / ORAL336 mgExact identifier — unii candidate
49 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, DELAYED RELEASE / ORAL2210 mgExact identifier — unii candidate
28 equally ranked IID candidates
POVIDONEPOVIDONEFZ989GH94ECAPSULE, COATED PELLETS / ORAL10.03 mgExact identifier — unii candidate
30 equally ranked IID candidates
ANHYDROUS LACTOSEANHYDROUS LACTOSE3SY5LH9PMKCAPSULE, DELAYED RELEASE / ORAL360 mgExact identifier — unii candidate
21 equally ranked IID candidates
SILICON DIOXIDESILICON DIOXIDEETJ7Z6XBU4POWDER, FOR SOLUTION / ORAL280 mgExact identifier — unii candidate
49 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 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINEASPIRIN; CAFFEINE; ORPHENADRINE CITRATE385MG;30MG;25MGTABLET / ORAL1996-12-31
A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINEASPIRIN; CAFFEINE; ORPHENADRINE CITRATE770MG;60MG;50MGTABLET / ORAL1996-12-31

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 3 · 86 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-3184e616aacf4f…
2026-09-14 22:38:342026-08A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-3184e616aacf4f…
2026-08-18 06:07:402026-07A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31caaa826d4ba7…
2026-08-18 06:07:402026-07A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31011fe1cb6892…
2026-02-19 14:30 UTC2026-02A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-3131067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-3131067a03dcf5…
2025-08-23 18:47 UTC2025-08A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-316a471c1ec25d…
2025-08-23 18:47 UTC2025-08A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-316a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-3103ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-3103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-312680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-312680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-315bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-315bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31d8e5a09893c0…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31d06236e962d9…
2024-10-29 15:01 UTC2024-10A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-3179d66fd596c7…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-3179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-31301d65b070ca…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-31301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-311e350fbaab3a…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-311e350fbaab3a…
2024-05-31 18:47 UTC2024-05A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-318072bd15b7f6…
2024-05-31 18:47 UTC2024-05A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-318072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-315c6f7cd8ea54…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-315c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-315d02ea3f76ae…
2022-04-08 23:34 UTC2022-04A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-315d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-314b0b4de00fa7…
2022-04-04 05:41 UTC2022-04A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORAL1996-12-314b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A074654-001ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE385MG;30MG;25MGTABLET / ORAL1996-12-3174a2ff9319b5…
2019-12-13 00:20 UTC2019-12A074654-002ORPHENADRINE CITRATE, ASPIRIN, AND CAFFEINE770MG;60MG;50MGTABLET / ORALABRS1996-12-3174a2ff9319b5…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2019-12-13 00:20 UTC2019-12A074654-002AB174a2ff9319b5…
2019-12-14 00:12 UTC2019-12A074654-002AB13f01610625f2…
2019-09-15 20:21 UTC2019-09A074654-002AB1b00525d2431f…
2019-07-19 19:46 UTC2019-07A074654-002AB1ea99ee380514…

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
8e41b33e-f71f-4a5e-b88f-cdfefb2bee208e41b33e-f71f-4a5e-b88f-cdfefb2bee202010-10-22Warnings, Adverse reactionsExact identifier
spl id: 8e41b33e-f71f-4a5e-b88f-cdfefb2bee20
spl set id: 8e41b33e-f71f-4a5e-b88f-cdfefb2bee20

Reported adverse events (FAERS/openFDA)#

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