fluphenazine hydrochloride

Generic: fluphenazine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluphenazine hydrochloride
Generic Name fluphenazine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fluphenazine hydrochloride 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-837
Product ID 71205-837_bc22941e-d2e7-4165-91ea-7239c8b9882d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215848
Listing Expiration 2026-12-31
Marketing Start 2022-08-01

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205837
Hyphenated Format 71205-837

Supplemental Identifiers

RxCUI
859841 860918 865117 865123
UPC
0371205839307 0371205837303 0371205838300 0371205840303
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
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-00)
  • 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-11)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-55)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-60)
  • 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-64)
  • 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-72)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-78)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-90)
source: ndc

Packages (9)

71205-837-00 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-00) 71205-837-11 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-11) 71205-837-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-30) 71205-837-55 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-55) 71205-837-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-60) 71205-837-64 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-64) 71205-837-72 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-72) 71205-837-78 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-78) 71205-837-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-90)

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": "bc22941e-d2e7-4165-91ea-7239c8b9882d", "openfda": {"upc": ["0371205839307", "0371205837303", "0371205838300", "0371205840303"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["bc22941e-d2e7-4165-91ea-7239c8b9882d"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-00)", "package_ndc": "71205-837-00", "marketing_start_date": "20230221"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-11)", "package_ndc": "71205-837-11", "marketing_start_date": "20230221"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-30)", "package_ndc": "71205-837-30", "marketing_start_date": "20230221"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-55)", "package_ndc": "71205-837-55", "marketing_start_date": "20230221"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-60)", "package_ndc": "71205-837-60", "marketing_start_date": "20230221"}, {"sample": false, "description": "240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-64)", "package_ndc": "71205-837-64", "marketing_start_date": "20230221"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-72)", "package_ndc": "71205-837-72", "marketing_start_date": "20230221"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-78)", "package_ndc": "71205-837-78", "marketing_start_date": "20230221"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-837-90)", "package_ndc": "71205-837-90", "marketing_start_date": "20230221"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "71205-837_bc22941e-d2e7-4165-91ea-7239c8b9882d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "71205-837", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA215848", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}