| NDC Code | 0378-6009-05 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6009-05) |
|---|
| Product NDC | 0378-6009 |
|---|
| 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 | 19880812 |
|---|
| End Marketing Date | 20201031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089804 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 2.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazines [CS],Phenothiazine [EPC] |
|---|