Package 71740-001-10

Brand: niacor

Generic: niacin
NDC Package

Package Facts

Identity

Package NDC 71740-001-10
Digits Only 7174000110
Product NDC 71740-001
Product ID 71740-001_800ff22d-b10c-4cc8-920f-217a4d23563d
Description

100 TABLET in 1 BOTTLE (71740-001-10)

Marketing

Marketing Status
Marketed Since 2021-12-16
Brand niacor
Generic niacin
Sample Package No

Linked Drug Pages (1)

Niacor ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "800ff22d-b10c-4cc8-920f-217a4d23563d", "openfda": {"nui": ["N0000175594", "M0014839"], "unii": ["2679MF687A"], "rxcui": ["198024", "311944"], "spl_set_id": ["bf287412-160b-403f-8eb4-57f29a475902"], "pharm_class_cs": ["Nicotinic Acids [CS]"], "pharm_class_epc": ["Nicotinic Acid [EPC]"], "manufacturer_name": ["Avondale Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71740-001-10)", "package_ndc": "71740-001-10", "marketing_start_date": "20211216"}], "brand_name": "Niacor", "product_id": "71740-001_800ff22d-b10c-4cc8-920f-217a4d23563d", "dosage_form": "TABLET", "pharm_class": ["Nicotinic Acid [EPC]", "Nicotinic Acids [CS]"], "product_ndc": "71740-001", "generic_name": "Niacin", "labeler_name": "Avondale Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Niacor", "active_ingredients": [{"name": "NIACIN", "strength": "500 mg/1"}], "application_number": "ANDA040378", "marketing_category": "ANDA", "marketing_start_date": "20000503", "listing_expiration_date": "20261231"}