fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: taro pharmaceuticals u.s.a. inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler taro pharmaceuticals u.s.a. inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 2.5 mg/1

Manufacturer
Taro Pharmaceuticals U.S.A. Inc.

Identifiers & Regulatory

Product NDC 51672-4234
Product ID 51672-4234_2e6cbcab-4d8a-5f9a-e063-6394a90a056c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215674
Listing Expiration 2026-12-31
Marketing Start 2022-04-14

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516724234
Hyphenated Format 51672-4234

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0351672423315 0351672423414 0351672423513
UNII
ZOU145W1XL

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fluphenazine hydrochloride (source: ndc)
Generic Name fluphenazine hydrochloride (source: ndc)
Application Number ANDA215674 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (51672-4234-1)
source: ndc

Packages (1)

51672-4234-1 100 TABLET, FILM COATED in 1 BOTTLE (51672-4234-1)

Ingredients (1)

fluphenazine hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Fluphenazine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2e6cbcab-4d8a-5f9a-e063-6394a90a056c", "openfda": {"upc": ["0351672423315", "0351672423414", "0351672423513"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["7036f7c6-0792-400d-a1c7-54f21b2bd481"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A. Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (51672-4234-1)", "package_ndc": "51672-4234-1", "marketing_start_date": "20220414"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "51672-4234_2e6cbcab-4d8a-5f9a-e063-6394a90a056c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51672-4234", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Taro Pharmaceuticals U.S.A. Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA215674", "marketing_category": "ANDA", "marketing_start_date": "20220414", "listing_expiration_date": "20261231"}