Fluphenazine Hydrochloride
- Product NDC
- 59651-687
- 11-digit product format
- 596510687
- Labeler code
- 59651
- Product ID
- 59651-687_1109b107-f7af-45b7-b8ee-709c59123074
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA218055
- Marketing category
- ANDA
- Marketing start
- 2023-08-18
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 2.5 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 | 2.5 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 |
|---|
| 59651-687-01 | Fluphenazine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59651-687 | FLUPHENAZINE HYDROCHLORIDE TABLET [AUROBINDO PHARMA LIMITED] | 3 | Current NDC, 1 package rows | 20241121_e73764e7-e666-4ad3-a029-04a528dc1c9e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59651-687-01 | 59651068701 | 100 TABLET in 1 BOTTLE (59651-687-01) | 100 tablet | 2023-08-18 | No | No | Historical |