| NDC Code | 58118-1437-0 |
|---|
| Package Description | 1 TABLET, FILM COATED in 1 PACKAGE (58118-1437-0) |
|---|
| Product NDC | 58118-1437 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluphenazine Hydrochloride |
|---|
| Non-Proprietary Name | Fluphenazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19871016 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089586 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 2.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
|---|