trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride

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

Drug Facts

Product Profile

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

trifluoperazine hydrochloride 10 mg/1

Manufacturer
Sandoz Inc.

Identifiers & Regulatory

Product NDC 0781-8036
Product ID 0781-8036_79bbd43c-c3f3-4fa5-a2a4-88868251febb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085788
Listing Expiration 2026-12-31
Marketing Start 1981-11-20

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07818036
Hyphenated Format 0781-8036

Supplemental Identifiers

RxCUI
198322 198323 198324 198325
UNII
6P1Y2SNF5V

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 trifluoperazine hydrochloride (source: ndc)
Generic Name trifluoperazine hydrochloride (source: ndc)
Application Number ANDA085788 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (0781-8036-01)
source: ndc

Packages (1)

0781-8036-01 100 TABLET, FILM COATED in 1 BOTTLE (0781-8036-01)

Ingredients (1)

trifluoperazine hydrochloride (10 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": "79bbd43c-c3f3-4fa5-a2a4-88868251febb", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198322", "198323", "198324", "198325"], "spl_set_id": ["ae43c10e-cfa9-4298-8af5-7a3e6524bbda"], "manufacturer_name": ["Sandoz Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-8036-01)", "package_ndc": "0781-8036-01", "marketing_start_date": "20190114"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "0781-8036_79bbd43c-c3f3-4fa5-a2a4-88868251febb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-8036", "generic_name": "Trifluoperazine Hydrochloride", "labeler_name": "Sandoz Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA085788", "marketing_category": "ANDA", "marketing_start_date": "19811120", "listing_expiration_date": "20261231"}