Trifluoperazine Hydrochloride
- Product NDC
- 70518-2015
- 11-digit product format
- 705182015
- Labeler code
- 70518
- Product ID
- 70518-2015_86d748ca-34a5-846e-e053-2a91aa0ad0ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trifluoperazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085785
- Marketing category
- ANDA
- Marketing start
- 2019-04-12
- Marketing end
- 0000-00-00
- Substance
- TRIFLUOPERAZINE HYDROCHLORIDE
- Active strength
- 1 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