NDC Code |
0093-5161-01 |
Proprietary Name |
Hydrocodone Bitartrate and Ibuprofen |
Package Description |
100 TABLET, FILM COATED in 1 BOTTLE (0093-5161-01) |
Product NDC |
0093-5161 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Hydrocodone Bitartrate and Ibuprofen |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20030415 |
Marketing Category Name |
ANDA |
Labeler Name |
Teva Pharmaceuticals USA Inc |
Substance Name |
HYDROCODONE BITARTRATE; IBUPROFEN |
Strength Number |
7.5; 200 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Opioid Agonist [EPC],Opioid Agonists [MoA],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |