NDC Code |
54868-5900-0 |
Proprietary Name |
Dihydrocodeine Bitartrate, Acetaminophen and Caffeine |
Package Description |
30 TABLET in 1 BOTTLE, PLASTIC (54868-5900-0) |
Product NDC |
54868-5900 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Dihydrocodeine Bitartrate, Acetaminophen and Caffeine |
Dosage Form Name |
TABLET |
Route Name |
ORAL |
Start Marketing Date |
20080520 |
Marketing Category Name |
ANDA |
Labeler Name |
Physicians Total Care, Inc. |
Substance Name |
ACETAMINOPHEN; CAFFEINE; DIHYDROCODEINE BITARTRATE |
Strength Number |
712.8; 60; 32 |
Strength Unit |
mg/1; mg/1; mg/1 |
Pharmaceutical Classes |
Full Opioid Agonists [MoA],Opioid Agonist [EPC],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |