Perphenazine
- Product NDC
- 70518-1717
- 11-digit product format
- 705181717
- Labeler code
- 70518
- Product ID
- 70518-1717_962fe44e-469b-dcb7-e053-2995a90a1bf7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 2018-12-07
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record