fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fluphenazine hydrochloride 10 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-369
Product ID 50268-369_2b499b3f-f98a-d07d-e063-6294a90ab453
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214534
Listing Expiration 2026-12-31
Marketing Start 2022-04-06

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268369
Hyphenated Format 50268-369

Supplemental Identifiers

RxCUI
859841
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 ANDA214534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-369-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-369-11)
source: ndc

Packages (1)

50268-369-15 50 BLISTER PACK in 1 BOX (50268-369-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-369-11)

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": "2b499b3f-f98a-d07d-e063-6294a90ab453", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841"], "spl_set_id": ["dbfd138a-e107-3f78-e053-2995a90a6d8c"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-369-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-369-11)", "package_ndc": "50268-369-15", "marketing_start_date": "20220406"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "50268-369_2b499b3f-f98a-d07d-e063-6294a90ab453", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50268-369", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214534", "marketing_category": "ANDA", "marketing_start_date": "20220406", "listing_expiration_date": "20261231"}