Fluphenazine hydrochloride
- Product NDC
- 51079-485
- 11-digit product format
- 510790485
- Labeler code
- 51079
- Product ID
- 51079-485_9c31c47b-4f7b-4800-e053-2a95a90ac060
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA089804
- Marketing category
- ANDA
- Marketing start
- 1998-04-30
- Marketing end
- 2020-06-30
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record