NDC Code | 68071-4749-6 |
Package Description | 60 TABLET in 1 BOTTLE (68071-4749-6) |
Product NDC | 68071-4749 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Acetaminophen And Codeine Phosphate |
Non-Proprietary Name | Acetaminophen And Codeine Phosphate |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20130415 |
Marketing Category Name | ANDA |
Application Number | ANDA202800 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength | 300; 60 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CIII |