NDC Code: |
0722-6670 |
Proprietary Name: |
Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
Suffix: |
|
Non-Proprietary Name: |
Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate |
Dosage Form: |
CAPSULE |
Method: |
ORAL |
Original Marketing Date: |
10-06-2004 |
Category Name: |
ANDA |
Application Number: |
ANDA076560 |
Labeler: |
NEXGEN PHARMA, INC. |
Substance Name: |
ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE |
Active Numerator Strength: |
325; 50; 40; 30 |
Active Ingredient Unit: |
mg/1; mg/1; mg/1; mg/1 |
Pharm Classes: |
Barbiturate [EPC],Barbiturates [Chemical/Ingredient],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule: |
CIII |