Fluphenazine Hydrochloride
- Product NDC
- 16714-672
- 11-digit product format
- 167140672
- Labeler code
- 16714
- Product ID
- 16714-672_941b9852-e201-488d-b959-382312335b21
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA214552
- Marketing category
- ANDA
- Marketing start
- 2021-11-24
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16714-672 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [NORTHSTAR RX LLC] | 4 | Legacy NDC | 20241207_6a87fecd-f339-430b-8943-02117ad70211.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-672-01 | 16714067201 | 100 TABLET, FILM COATED in 1 BOTTLE (16714-672-01) | 2021-11-24 | 0000-00-00 | No | No | Current |