NDC Code | 60760-032-40 |
Package Description | 40 TABLET in 1 BOTTLE, PLASTIC (60760-032-40) |
Product NDC | 60760-032 |
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 | 20060119 |
End Marketing Date | 20191130 |
Marketing Category Name | ANDA |
Application Number | ANDA040656 |
Manufacturer | St. Mary's Medical Park Pharmacy |
Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
Strength | 7.5; 325 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
DEA Schedule | CII |