NDC 51672-4235 – Fluphenazine Hydrochloride
Fluphenazine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC51672-4235
Product details
- Brand name
- Fluphenazine Hydrochloride
- Generic name
- Fluphenazine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215674
- Marketed since
- April 14, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Phenothiazine
Active ingredients
- Fluphenazine Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Fluphenazine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4235-1 | 100 TABLET, FILM COATED in 1 BOTTLE (51672-4235-1) | Apr 14, 2022 |
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