fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fluphenazine hydrochloride 1 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1567
Product ID 67046-1567_37c96bed-4f7d-8a59-e063-6294a90a3d58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218173
Listing Expiration 2026-12-31
Marketing Start 2025-06-17

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461567
Hyphenated Format 67046-1567

Supplemental Identifiers

RxCUI
865117
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 ANDA218173 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1567-3)
source: ndc

Packages (1)

67046-1567-3 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1567-3)

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": "37c96bed-4f7d-8a59-e063-6294a90a3d58", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["865117"], "spl_set_id": ["37c9712b-95a1-fcc4-e063-6394a90aca50"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1567-3)", "package_ndc": "67046-1567-3", "marketing_start_date": "20250617"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "67046-1567_37c96bed-4f7d-8a59-e063-6294a90a3d58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1567", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}