NDC Code | 49999-609-01 |
Package Description | 120 TABLET in 1 BOTTLE (49999-609-01) |
Product NDC | 49999-609 |
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 | 20111109 |
Marketing Category Name | ANDA |
Application Number | ANDA040405 |
Manufacturer | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
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 | CIII |