Fluphenazine Hydrochloride 51672-4233
Product NDC
51672-4233- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 14, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA215674
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Fluphenazine Hydrochloride | 1 mg/1 |
Drug Class
Phenothiazine [EPC]Phenothiazines [CS]
Packaging Options(1)
1 BOTTLE in 1 CARTON (51672-4233-1) / 100 TABLET, FILM COATED in 1 BOTTLE