niacor
Generic: niacin
Labeler: avondale pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
niacor
Generic Name
niacin
Labeler
avondale pharmaceuticals, llc
Dosage Form
TABLET
Routes
Active Ingredients
niacin 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71740-001
Product ID
71740-001_800ff22d-b10c-4cc8-920f-217a4d23563d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040378
Listing Expiration
2026-12-31
Marketing Start
2000-05-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71740001
Hyphenated Format
71740-001
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
niacor (source: ndc)
Generic Name
niacin (source: ndc)
Application Number
ANDA040378 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (71740-001-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}