Fluphenazine Hydrochloride
- Product NDC
- 71205-837
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA215848
- Marketing category
- ANDA
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-837-00 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-00) | 2023-02-21 | | No | Historical |
| 71205-837-11 | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-11) | 2023-02-21 | | No | Historical |
| 71205-837-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-30) | 2023-02-21 | | No | Historical |
| 71205-837-55 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-55) | 2023-02-21 | | No | Historical |
| 71205-837-60 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-60) | 2023-02-21 | | No | Historical |
| 71205-837-64 | 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-64) | 2023-02-21 | | No | Historical |
| 71205-837-72 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-72) | 2023-02-21 | | No | Historical |
| 71205-837-78 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-78) | 2023-02-21 | | No | Historical |
| 71205-837-90 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-90) | 2023-02-21 | | No | Historical |