fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler ajanta pharma usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 1 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-255
Product ID 27241-255_0069bda4-a743-4edd-a15f-a53cba1a2bff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217410
Listing Expiration 2027-12-31
Marketing Start 2023-01-05

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241255
Hyphenated Format 27241-255

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0327241255014 0327241252013 0327241253010 0327241254017
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 ANDA217410 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (27241-255-01)
source: ndc

Packages (1)

27241-255-01 100 TABLET in 1 BOTTLE (27241-255-01)

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": "0069bda4-a743-4edd-a15f-a53cba1a2bff", "openfda": {"upc": ["0327241255014", "0327241252013", "0327241253010", "0327241254017"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["47695e20-9c0b-4a6b-ab1a-1dfaa75e96d8"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (27241-255-01)", "package_ndc": "27241-255-01", "marketing_start_date": "20230105"}], "brand_name": "Fluphenazine hydrochloride", "product_id": "27241-255_0069bda4-a743-4edd-a15f-a53cba1a2bff", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "27241-255", "generic_name": "Fluphenazine hydrochloride", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA217410", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20271231"}