Trifluoperazine Hydrochloride
- Product NDC
- 0832-0497
- 11-digit product format
- 008320497
- Labeler code
- 0832
- Product ID
- 0832-0497_72461ed1-9688-4782-9533-25d9b07c2de7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trifluoperazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA085788
- Marketing category
- ANDA
- Marketing start
- 2015-03-09
- Marketing end
- 2022-06-30
- Substance
- TRIFLUOPERAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0832-0497-11 | 00832049711 | 100 TABLET, FILM COATED in 1 BOTTLE (0832-0497-11) | 2015-03-09 | 2022-06-30 | No | No | Current |