Package 0173-0889-39
Brand: krintafel
Generic: tafenoquine succinatePackage Facts
Identity
Package NDC
0173-0889-39
Digits Only
0173088939
Product NDC
0173-0889
Description
2 TABLET, FILM COATED in 1 BOTTLE (0173-0889-39)
Marketing
Marketing Status
Brand
krintafel
Generic
tafenoquine succinate
Sample Package
No
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"}