| NDC Code |
64376-611-31 |
| Proprietary Name |
Acetaminophen, Caffeine and Dihydrocodeine Bitartrate |
| Package Description |
30 TABLET in 1 BOTTLE (64376-611-31) |
| Product NDC |
64376-611 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
Acetaminophen, Caffeine and Dihydrocodeine Bitartrate |
| Dosage Form Name |
TABLET |
| Route Name |
ORAL |
| Start Marketing Date |
20070403 |
| Marketing Category Name |
ANDA |
| Labeler Name |
Boca Pharmacal, Inc. |
| Substance Name |
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE |
| Strength Number |
712.8; 60; 32 |
| Strength Unit |
mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient],Full Opioid Agonists [MoA],Opioid Agonist [EPC] |