trifluoperazine hydrochloride

Generic: trifluoperazine hydrochloride

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

Drug Facts

Product Profile

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

trifluoperazine hydrochloride 2 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2095
Product ID 70518-2095_499dd16d-513b-780e-e063-6294a90a0230
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040209
Listing Expiration 2027-12-31
Marketing Start 2019-05-21

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182095
Hyphenated Format 70518-2095

Supplemental Identifiers

RxCUI
198324
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
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0)
source: ndc

Packages (1)

70518-2095-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0)

Ingredients (1)

trifluoperazine hydrochloride (2 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": "499dd16d-513b-780e-e063-6294a90a0230", "openfda": {"unii": ["6P1Y2SNF5V"], "rxcui": ["198324"], "spl_set_id": ["339ceb53-3b1c-459f-84eb-77bd4315c998"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0)", "package_ndc": "70518-2095-0", "marketing_start_date": "20190521"}], "brand_name": "Trifluoperazine Hydrochloride", "product_id": "70518-2095_499dd16d-513b-780e-e063-6294a90a0230", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-2095", "generic_name": "trifluoperazine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trifluoperazine Hydrochloride", "active_ingredients": [{"name": "TRIFLUOPERAZINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA040209", "marketing_category": "ANDA", "marketing_start_date": "20190521", "listing_expiration_date": "20271231"}