NDC Code | 60760-870-60 |
Package Description | 60 TABLET in 1 BOTTLE, PLASTIC (60760-870-60) |
Product NDC | 60760-870 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Non-Proprietary Name | Hydrocodone Bitartrate And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20001020 |
Marketing Category Name | ANDA |
Application Number | ANDA040409 |
Manufacturer | ST. MARY'S MEDICAL PARK PHARMACY |
Substance Name | ACETAMINOPHEN; HYDROCODONE BITARTRATE |
Strength | 325; 5 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Opioid Agonist [EPC], Opioid Agonists [MoA] |
DEA Schedule | CII |