Fluphenazine Hydrochloride
- Product NDC
- 51407-461
- 11-digit product format
- 514070461
- Labeler code
- 51407
- Product ID
- 51407-461_2bb360b2-0a94-4e45-e063-6294a90afca7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA214534
- Marketing category
- ANDA
- Marketing start
- 2021-01-07
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluphenazine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUPHENAZINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | ZOU145W1XL |
| Rxcui | 859841, 860918, 865117, 865123 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-461-01 | Fluphenazine Hydrochloride | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-461 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250119_c2c6d6a1-b4b9-506d-e053-2995a90aac23.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-461-01 | 51407046101 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-461-01) | 2021-03-03 | 0000-00-00 | No | No | Current |