fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

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

Drug Facts

Product Profile

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

fluphenazine hydrochloride 1 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-384
Product ID 31722-384_4468c081-e6a4-bbbf-e063-6294a90aa886
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218769
Listing Expiration 2026-12-31
Marketing Start 2025-11-18

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722384
Hyphenated Format 31722-384

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0331722386012 0331722387019 0331722385015
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 ANDA218769 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (31722-384-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-384-05)
source: ndc

Packages (2)

31722-384-01 100 TABLET, FILM COATED in 1 BOTTLE (31722-384-01) 31722-384-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-384-05)

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": "4468c081-e6a4-bbbf-e063-6294a90aa886", "openfda": {"upc": ["0331722386012", "0331722387019", "0331722385015"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["4dd61338-8e4b-41c6-99d8-811a8e990c4e"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-384-01)", "package_ndc": "31722-384-01", "marketing_start_date": "20251118"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-384-05)", "package_ndc": "31722-384-05", "marketing_start_date": "20251118"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "31722-384_4468c081-e6a4-bbbf-e063-6294a90aa886", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "31722-384", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA218769", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}