fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

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

Drug Facts

Product Profile

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

fluphenazine hydrochloride 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3707
Product ID 70518-3707_3b122509-7283-b29e-e063-6294a90a3903
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215848
Listing Expiration 2026-12-31
Marketing Start 2023-04-10

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183707
Hyphenated Format 70518-3707

Supplemental Identifiers

RxCUI
860918
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 ANDA215848 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3707-0)
source: ndc

Packages (1)

70518-3707-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3707-0)

Ingredients (1)

fluphenazine hydrochloride (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": "3b122509-7283-b29e-e063-6294a90a3903", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["860918"], "spl_set_id": ["f68bacd4-3205-4735-996f-9e953e83cf48"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3707-0)", "package_ndc": "70518-3707-0", "marketing_start_date": "20230410"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70518-3707_3b122509-7283-b29e-e063-6294a90a3903", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-3707", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215848", "marketing_category": "ANDA", "marketing_start_date": "20230410", "listing_expiration_date": "20261231"}