Fluphenazine Hydrochloride
- Product NDC
- 42291-436
- 11-digit product format
- 422910436
- Labeler code
- 42291
- Product ID
- 42291-436_d57cc326-d857-0598-e053-2995a90acd95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA089743
- Marketing category
- ANDA
- Marketing start
- 2020-09-21
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-436-01 | 42291043601 | 100 TABLET, FILM COATED in 1 BOTTLE (42291-436-01) | 2020-09-21 | 0000-00-00 | No | No | Current |