fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

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

Drug Facts

Product Profile

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

fluphenazine hydrochloride 5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-275
Product ID 70954-275_b62e66ce-9c80-46f1-bb86-68f7f73c487c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214674
Listing Expiration 2026-12-31
Marketing Start 2021-03-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70954275
Hyphenated Format 70954-275

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0370954275107 0370954276104 0370954276203 0370954275206 0370954273103
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 ANDA214674 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70954-275-10)
  • 500 TABLET in 1 BOTTLE (70954-275-20)
source: ndc

Packages (2)

70954-275-10 100 TABLET in 1 BOTTLE (70954-275-10) 70954-275-20 500 TABLET in 1 BOTTLE (70954-275-20)

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": "b62e66ce-9c80-46f1-bb86-68f7f73c487c", "openfda": {"upc": ["0370954275107", "0370954276104", "0370954276203", "0370954275206", "0370954273103"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["6218cbd2-1f7f-40fa-92d2-5d5b0d7fa60b"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-275-10)", "package_ndc": "70954-275-10", "marketing_start_date": "20210301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70954-275-20)", "package_ndc": "70954-275-20", "marketing_start_date": "20210301"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70954-275_b62e66ce-9c80-46f1-bb86-68f7f73c487c", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70954-275", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA214674", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}