Fluphenazine Hydrochloride
- Product NDC
- 70771-1581
- 11-digit product format
- 707711581
- Labeler code
- 70771
- Product ID
- 70771-1581_1db40261-ae57-4539-a7e9-7ca75d96627a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA214552
- Marketing category
- ANDA
- Marketing start
- 2021-05-28
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| ZOU145W1XL | FLUPHENAZINE HYDROCHLORIDE | 146-56-5 | FLUPHENAZINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1581-1 | 70771158101 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1581-1) | 2021-05-28 | No | No | Historical |
| 70771-1581-5 | 70771158105 | 500 TABLET, FILM COATED in 1 BOTTLE (70771-1581-5) | 2021-05-28 | No | No | Historical |