Fluphenazine Hydrochloride
- Product NDC
- 51672-4235
- 11-digit product format
- 516724235
- Labeler code
- 51672
- Product ID
- 51672-4235_4db5cdb5-b848-695f-e063-6294a90a25b5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA215674
- Marketing category
- ANDA
- Marketing start
- 2022-04-14
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluphenazine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUPHENAZINE HYDROCHLORIDE | 5 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 |
|---|
| 51672-4235-1 | Fluphenazine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51672-4235 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [TARO PHARMACEUTICALS U.S.A. INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250303_7036f7c6-0792-400d-a1c7-54f21b2bd481.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 |
|---|
| 51672-4235-1 | 51672423501 | 100 TABLET, FILM COATED in 1 BOTTLE (51672-4235-1) | 2022-04-14 | 0000-00-00 | No | No | Current |