trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trifluoperazine hydrochloride
Generic Name trifluoperazine hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

trifluoperazine hydrochloride 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2207
Product ID 72162-2207_7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085789
Marketing Start 1981-11-20
Marketing End 2027-03-19

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622207
Hyphenated Format 72162-2207

Supplemental Identifiers

RxCUI
198325
UNII
6P1Y2SNF5V

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 trifluoperazine hydrochloride (source: ndc)
Generic Name trifluoperazine hydrochloride (source: ndc)
Application Number ANDA085789 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (72162-2207-1)
source: ndc

Packages (1)

72162-2207-1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2207-1)

Ingredients (1)

trifluoperazine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Trifluoperazine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198325"], "spl_set_id": ["7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2207-1)", "package_ndc": "72162-2207-1", "marketing_end_date": "20270319", "marketing_start_date": "20240402"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "72162-2207_7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72162-2207", "generic_name": "Trifluoperazine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA085789", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "19811120"}