| NDC Code | 16571-890-50 |
|---|
| Package Description | 500 TABLET, FILM COATED in 1 CONTAINER (16571-890-50) |
|---|
| Product NDC | 16571-890 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Fluphenazine Hydrochoride |
|---|
| Non-Proprietary Name | Fluphenazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240607 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA218283 |
|---|
| Manufacturer | Rising Pharma Holdings, Inc. |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 2.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|