krintafel

Generic: tafenoquine succinate

Labeler: glaxosmithkline llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name krintafel
Generic Name tafenoquine succinate
Labeler glaxosmithkline llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

tafenoquine succinate 150 mg/1

Manufacturer
GlaxoSmithKline LLC

Identifiers & Regulatory

Product NDC 0173-0889
Product ID 0173-0889_ebe22603-a38f-475d-a2b6-9ffe00dbcd23
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA210795
Listing Expiration 2026-12-31
Marketing Start 2019-01-22

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01730889
Hyphenated Format 0173-0889

Supplemental Identifiers

RxCUI
2109233 2109239
UPC
0301730889393
UNII
DL5J0B8VSS

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 krintafel (source: ndc)
Generic Name tafenoquine succinate (source: ndc)
Application Number NDA210795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 2 TABLET, FILM COATED in 1 BOTTLE (0173-0889-39)
source: ndc

Packages (1)

Ingredients (1)

tafenoquine succinate (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ebe22603-a38f-475d-a2b6-9ffe00dbcd23", "openfda": {"upc": ["0301730889393"], "unii": ["DL5J0B8VSS"], "rxcui": ["2109233", "2109239"], "spl_set_id": ["5cf989d5-36f5-4561-a30b-9fcb9deb6b6a"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (0173-0889-39)", "package_ndc": "0173-0889-39", "marketing_start_date": "20190122"}], "brand_name": "Krintafel", "product_id": "0173-0889_ebe22603-a38f-475d-a2b6-9ffe00dbcd23", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0173-0889", "generic_name": "tafenoquine succinate", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Krintafel", "active_ingredients": [{"name": "TAFENOQUINE SUCCINATE", "strength": "150 mg/1"}], "application_number": "NDA210795", "marketing_category": "NDA", "marketing_start_date": "20190122", "listing_expiration_date": "20261231"}