fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 10 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7160
Product ID 0904-7160_491d902d-1778-4bd3-a836-d1faf6ea9930
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089743
Listing Expiration 2026-12-31
Marketing Start 1988-08-25

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047160
Hyphenated Format 0904-7160

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UNII
ZOU145W1XL

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 ANDA089743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7160-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7160-61 100 BLISTER PACK in 1 CARTON (0904-7160-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

fluphenazine hydrochloride (10 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": "491d902d-1778-4bd3-a836-d1faf6ea9930", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["e8d4065a-45fc-4adf-9406-2122ca131d99"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7160-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7160-61", "marketing_start_date": "19880825"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0904-7160_491d902d-1778-4bd3-a836-d1faf6ea9930", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0904-7160", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA089743", "marketing_category": "ANDA", "marketing_start_date": "19880825", "listing_expiration_date": "20261231"}