| NDC Code | 68084-950-21 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-950-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-950-11) |
|---|
| Product NDC | 68084-950 |
|---|
| 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 | 20150331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA089742 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
|---|