Fluphenazine Hydrochloride
- Product NDC
- 0832-6006
- 11-digit product format
- 008326006
- Labeler code
- 0832
- Product ID
- 0832-6006_3bb74f82-8872-9829-e063-6294a90aeace
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories,LLC
- Application
- ANDA213784
- Marketing category
- ANDA
- Marketing start
- 2022-11-22
- Marketing end
- 2027-07-31
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Fluphenazine Hydrochloride
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 |
|---|
| 0832-6006-11 | Fluphenazine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0832-6006 | FLUPHENAZINE HYDROCHLORIDE TABLET, FILM COATED [UPSHER-SMITH LABORATORIES,LLC] | 3 | Current NDC, 1 package rows | 20240716_f07bb3f1-c68c-441b-9de4-99a219f2500a.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 |
|---|
| 0832-6006-11 | 00832600611 | 100 TABLET, FILM COATED in 1 BOTTLE (0832-6006-11) | 2023-03-02 | 2027-07-31 | No | No | Historical |