| NDC Code | 24979-138-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-138-01) |
|---|
| Product NDC | 24979-138 |
|---|
| 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 | 20220801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA215848 |
|---|
| Manufacturer | TWi Pharmaceuticals, Inc. |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|