fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: dr. reddys laboratories inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

fluphenazine hydrochloride 1 mg/1

Manufacturer
Dr. Reddys Laboratories Inc.

Identifiers & Regulatory

Product NDC 43598-034
Product ID 43598-034_95c5a977-cf1e-488a-8eff-c5fabc4b73c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214534
Listing Expiration 2026-12-31
Marketing Start 2021-02-15

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43598034
Hyphenated Format 43598-034

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0343598037011 0343598036014 0343598034010 0343598035017
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 ANDA214534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43598-034-01)
source: ndc

Packages (1)

43598-034-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43598-034-01)

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": "95c5a977-cf1e-488a-8eff-c5fabc4b73c3", "openfda": {"upc": ["0343598037011", "0343598036014", "0343598034010", "0343598035017"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["98aeddfd-4f24-4d1a-820d-d0abc1733794"], "manufacturer_name": ["Dr. Reddys Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43598-034-01)", "package_ndc": "43598-034-01", "marketing_start_date": "20210215"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "43598-034_95c5a977-cf1e-488a-8eff-c5fabc4b73c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "43598-034", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Dr. Reddys Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA214534", "marketing_category": "ANDA", "marketing_start_date": "20210215", "listing_expiration_date": "20261231"}