fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 1 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 70710-1488
Product ID 70710-1488_130b45fa-6dbd-46cc-a937-ab8ef1ec0718
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214552
Listing Expiration 2026-12-31
Marketing Start 2021-05-28

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101488
Hyphenated Format 70710-1488

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
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 ANDA214552 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1)
  • 500 TABLET, FILM COATED in 1 BOTTLE (70710-1488-5)
source: ndc

Packages (2)

70710-1488-1 100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1) 70710-1488-5 500 TABLET, FILM COATED in 1 BOTTLE (70710-1488-5)

Ingredients (1)

fluphenazine hydrochloride (1 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": "130b45fa-6dbd-46cc-a937-ab8ef1ec0718", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["c4448579-3ccb-442e-8950-a219d1f01a98"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1)", "package_ndc": "70710-1488-1", "marketing_start_date": "20210528"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1488-5)", "package_ndc": "70710-1488-5", "marketing_start_date": "20210528"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70710-1488_130b45fa-6dbd-46cc-a937-ab8ef1ec0718", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1488", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA214552", "marketing_category": "ANDA", "marketing_start_date": "20210528", "listing_expiration_date": "20261231"}