Fluphenazine Hydrochloride
- Product NDC
- 53808-0600
- 11-digit product format
- 538080600
- Labeler code
- 53808
- Product ID
- 53808-0600_4589f1cd-5570-48bb-a94b-499faa06d4a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUPHENAZINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA089804
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#