Fluphenazine Hydrochloride 68462-0914
Product NDC
68462-0914- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 6, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA216350
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluphenazine Hydrochloride | 1 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-914-01)
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-914-05)
100 BLISTER PACK in 1 CARTON (68462-914-14) / 1 TABLET, FILM COATED in 1 BLISTER PACK