NDC 16571-890 – Fluphenazine Hydrochoride
Fluphenazine Hydrochloride 2.5 mg/1 · Tablet, Film Coated · Oral
Product NDC16571-890
Product details
- Brand name
- Fluphenazine Hydrochoride
- Generic name
- Fluphenazine hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA218283
- Marketed since
- June 7, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Phenothiazine
Active ingredients
- Fluphenazine Hydrochloride 2.5 mg/1
Uses, dosage, side effects and warnings for Fluphenazine Hydrochoride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16571-890-09 | 90 TABLET, FILM COATED in 1 CONTAINER (16571-890-09) | Jun 7, 2024 |
| 16571-890-50 | 500 TABLET, FILM COATED in 1 CONTAINER (16571-890-50) | Jun 7, 2024 |
Other Fluphenazine Hydrochoride products
- 70518-4691 Fluphenazine Hydrochloride 10 mg/1 · Tablet, Film Coated · REMEDYREPACK INC.
- 16571-889 Fluphenazine Hydrochloride 1 mg/1 · Tablet, Film Coated · Rising Pharma Holdings, Inc.
- 16571-891 Fluphenazine Hydrochloride 5 mg/1 · Tablet, Film Coated · Rising Pharma Holdings, Inc.
- 16571-892 Fluphenazine Hydrochloride 10 mg/1 · Tablet, Film Coated · Rising Pharma Holdings, Inc.