Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Butalbital; Acetaminophen; Caffeine; Codeine Phosphate.
Product ID | 71335-0653_a29db87b-3f50-40ca-a5ab-406028ff19f0 |
NDC | 71335-0653 |
Product Type | Human Prescription Drug |
Proprietary Name | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
Generic Name | Butalbital, Acetaminophen, Caffeine, And Codeine Phosphate |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2002-04-22 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075929 |
Labeler Name | Bryant Ranch Prepack |
Substance Name | BUTALBITAL; ACETAMINOPHEN; CAFFEINE; CODEINE PHOSPHATE |
Active Ingredient Strength | 50 mg/1; mg/1; mg/1; mg/1 |
Pharm Classes | Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CIII |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2018-01-25 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075929 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-01-25 |
Marketing End Date | 2019-07-31 |
Ingredient | Strength |
---|---|
BUTALBITAL | 50 mg/1 |
SPL SET ID: | 00431d9b-fe0b-4aab-9d18-ac6ee6b9d6fe |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0591-2641 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
0591-3220 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
0603-2553 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
0722-6670 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
0722-7028 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
63629-3152 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
71335-0653 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
79739-6670 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
79739-7028 | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
52544-082 | Fioricet with Codeine | Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |