| NDC Code | 23155-012-01 |
|---|
| Package Description | 100 CAPSULE in 1 BOTTLE (23155-012-01) |
|---|
| Product NDC | 23155-012 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Propoxyphene Hydrochloride |
|---|
| Non-Proprietary Name | Propoxyphene Hydrochloride |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090501 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA080530 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc |
|---|
| Substance Name | PROPOXYPHENE HYDROCHLORIDE |
|---|
| Strength | 65 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
|---|
| DEA Schedule | CIV |
|---|