Trifluoperazine Hydrochloride
- Product NDC
- 35356-823
- 11-digit product format
- 353560823
- Labeler code
- 35356
- Product ID
- 35356-823_55a9cb2a-2c00-4e4a-adce-d48cc6ce1b23
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- trifluoperazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040209
- Marketing category
- ANDA
- Marketing start
- 2012-08-22
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record