fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler novadoz pharmaceuticals llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 10 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-115
Product ID 72205-115_f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217189
Listing Expiration 2026-12-31
Marketing Start 2023-09-11

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205115
Hyphenated Format 72205-115

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0372205115910 0372205114913 0372205112919 0372205113916 0372205114050 0372205112056 0372205113053
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 ANDA217189 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-05)
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-91)
source: ndc

Packages (2)

72205-115-05 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-05) 72205-115-91 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-91)

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": "f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82", "openfda": {"upc": ["0372205115910", "0372205114913", "0372205112919", "0372205113916", "0372205114050", "0372205112056", "0372205113053"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["83ce71b9-28eb-4074-b1e7-192ed254c529"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-05)", "package_ndc": "72205-115-05", "marketing_start_date": "20230914"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72205-115-91)", "package_ndc": "72205-115-91", "marketing_start_date": "20230914"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "72205-115_f99e9ea5-3c4a-4a94-9ca9-709f65b8fd82", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72205-115", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA217189", "marketing_category": "ANDA", "marketing_start_date": "20230911", "listing_expiration_date": "20261231"}