FLUPHENAZINE HYDROCHLORIDE
- Product NDC
- 10135-728
- 11-digit product format
- 101350728
- Labeler code
- 10135
- Product ID
- 10135-728_437e142c-e2e3-2b97-e063-6294a90a9266
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUPHENAZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Marlex Pharmaceuticals, Inc.
- Application
- ANDA214674
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- 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 |
|---|
| 10135-728-01 | FLUPHENAZINE HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-728 | FLUPHENAZINE HYDROCHLORIDE TABLET [MARLEX PHARMACEUTICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241009_c69f07b1-660c-db03-e053-2995a90a5464.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 |
|---|
| 10135-728-01 | 10135072801 | 100 TABLET in 1 BOTTLE (10135-728-01) | 100 tablet | 2021-06-01 | 0000-00-00 | No | No | Current |