fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fluphenazine hydrochloride 10 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1791
Product ID 0527-1791_59cf1ea7-b827-4780-bf94-cd3446d6dcc3
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 05271791
Hyphenated Format 0527-1791

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0305271791016 0305271790019 0305271789013
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 ANDA089743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)
source: ndc

Packages (2)

0527-1791-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-01) 0527-1791-05 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)

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": "59cf1ea7-b827-4780-bf94-cd3446d6dcc3", "openfda": {"upc": ["0305271791016", "0305271790019", "0305271789013"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["6cd6ba35-3481-48c1-87db-dc74ce9d7d75"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-01)", "package_ndc": "0527-1791-01", "marketing_start_date": "19880825"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1791-05)", "package_ndc": "0527-1791-05", "marketing_start_date": "19880825"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0527-1791_59cf1ea7-b827-4780-bf94-cd3446d6dcc3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0527-1791", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "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"}