trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride

Labeler: mylan institutional inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name trifluoperazine hydrochloride
Generic Name trifluoperazine hydrochloride
Labeler mylan institutional inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

trifluoperazine hydrochloride 1 mg/1

Manufacturer
Mylan Institutional Inc.

Identifiers & Regulatory

Product NDC 51079-572
Product ID 51079-572_3a877366-459b-cfac-e063-6294a90a6453
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040209
Listing Expiration 2026-12-31
Marketing Start 1998-03-04

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51079572
Hyphenated Format 51079-572

Supplemental Identifiers

RxCUI
198322 198323 198324 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 ANDA040209 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (51079-572-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)
source: ndc

Packages (1)

Ingredients (1)

trifluoperazine hydrochloride (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3a877366-459b-cfac-e063-6294a90a6453", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["f742a579-411a-4140-91c4-edc735d638fa"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-572-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-572-01)", "package_ndc": "51079-572-20", "marketing_start_date": "19980304"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "51079-572_3a877366-459b-cfac-e063-6294a90a6453", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "51079-572", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "19980304", "listing_expiration_date": "20261231"}