fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: alembic pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fluphenazine hydrochloride 2.5 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-789
Product ID 62332-789_f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218173
Listing Expiration 2026-12-31
Marketing Start 2024-07-25

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332789
Hyphenated Format 62332-789

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0362332790319 0362332788316 0362332789313 0362332791316
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 ANDA218173 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (62332-789-31)
  • 500 TABLET, FILM COATED in 1 BOTTLE (62332-789-71)
source: ndc

Packages (2)

62332-789-31 100 TABLET, FILM COATED in 1 BOTTLE (62332-789-31) 62332-789-71 500 TABLET, FILM COATED in 1 BOTTLE (62332-789-71)

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": "f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4", "openfda": {"upc": ["0362332790319", "0362332788316", "0362332789313", "0362332791316"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["1991be2c-9629-4c3e-93f0-e40bcffc82b0"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62332-789-31)", "package_ndc": "62332-789-31", "marketing_start_date": "20240725"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62332-789-71)", "package_ndc": "62332-789-71", "marketing_start_date": "20240725"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "62332-789_f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "62332-789", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20240725", "listing_expiration_date": "20261231"}