Fluphenazine hydrochloride
- Product NDC
- 27241-252
- 11-digit product format
- 272410252
- Labeler code
- 27241
- Product ID
- 27241-252_0069bda4-a743-4edd-a15f-a53cba1a2bff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ajanta Pharma USA Inc.
- Application
- ANDA217410
- Marketing category
- ANDA
- Marketing start
- 2023-01-05
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 10 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 | 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 |
|---|
| 27241-252-01 | Fluphenazine hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 27241-252 | FLUPHENAZINE HYDROCHLORIDE TABLET [AJANTA PHARMA USA INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241204_47695e20-9c0b-4a6b-ab1a-1dfaa75e96d8.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 |
|---|
| 27241-252-01 | 27241025201 | 100 TABLET in 1 BOTTLE (27241-252-01) | 100 tablet | 2023-01-05 | 0000-00-00 | No | No | Current |