fluphenazine hydrochloride
- Product NDC
- 16714-002
- 11-digit product format
- 167140002
- Labeler code
- 16714
- Product ID
- 16714-002_ce1c174a-201a-4911-9ad5-0a28034cf2eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluphenazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA213647
- Marketing category
- ANDA
- Marketing start
- 2021-03-03
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- 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 |
|---|
| 16714-002-01 | 16714000201 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16714-002-01) | 2021-03-03 | 0000-00-00 | No | No | Current |