Fluphenazine Hydrochloride
- Product NDC
- 50090-4740
- 11-digit product format
- 500904740
- Labeler code
- 50090
- Product ID
- 50090-4740_35cfc41e-9f13-4b10-a015-5643cb5d6074
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA089743
- Marketing category
- ANDA
- Marketing start
- 1988-08-25
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 5 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4740-0 | Fluphenazine Hydrochloride | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 3 |
| 50090-4740-0 | Fluphenazine Hydrochloride | 32 in 1 CARTON | TABLET, FILM COATED | 32 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4740 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20210416_a8360aca-5f69-4ad0-b2ed-99a66b601198.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4740-0 | 50090474000 | 32 BLISTER PACK in 1 CARTON (50090-4740-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 32 blister pack | 2019-11-20 | 0000-00-00 | No | No | Current |