| NDC Code | 63874-201-60 |
|---|
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63874-201-60) |
|---|
| Product NDC | 63874-201 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propoxyphene And Acetaminophen |
|---|
| Non-Proprietary Name | Propoxyphene Napsylate And Acetaminophen |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074843 |
|---|
| Manufacturer | Altura Pharmaceuticals, Inc. |
|---|
| Substance Name | PROPOXYPHENE NAPSYLATE; ACETAMINOPHEN |
|---|
| Strength | 100; 650 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
|---|
| DEA Schedule | CIV |
|---|