NDC Code | 54868-0072-9 |
Package Description | 10 TABLET in 1 BOTTLE (54868-0072-9) |
Product NDC | 54868-0072 |
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 | 20030925 |
Marketing Category Name | ANDA |
Application Number | ANDA040419 |
Manufacturer | Physicians Total Care, Inc. |
Substance Name | ACETAMINOPHEN; CODEINE PHOSPHATE |
Strength | 300; 30 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CIII |