fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 1 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-136
Product ID 24979-136_e2589baf-4d61-4d50-a578-41c51fbb6deb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215848
Listing Expiration 2026-12-31
Marketing Start 2022-08-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24979136
Hyphenated Format 24979-136

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0324979139012 0324979138015 0324979137018 0324979136011
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 ANDA215848 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-136-01)
source: ndc

Packages (1)

24979-136-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-136-01)

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": "e2589baf-4d61-4d50-a578-41c51fbb6deb", "openfda": {"upc": ["0324979139012", "0324979138015", "0324979137018", "0324979136011"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["d0a090fa-f7c9-4f6d-a9a3-9838870c7049"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-136-01)", "package_ndc": "24979-136-01", "marketing_start_date": "20220801"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "24979-136_e2589baf-4d61-4d50-a578-41c51fbb6deb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "24979-136", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA215848", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}