| NDC Code | 0093-0350-01 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (0093-0350-01) |
|---|
| Product NDC | 0093-0350 |
|---|
| 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 | 19900930 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA088629 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, 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 |
|---|