NDC Code | 49999-053-10 |
Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (49999-053-10) |
Product NDC | 49999-053 |
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 | 20111103 |
Marketing Category Name | ANDA |
Application Number | ANDA040201 |
Manufacturer | Lake Erie Medical &Surgical Supply DBA Quality Care Products LLC |
Substance Name | HYDROCODONE BITARTRATE; ACETAMINOPHEN |
Strength | 7.5; 500 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Opioid Agonist [EPC],Opioid Agonists [MoA] |
DEA Schedule | CIII |