niacin

Generic: niacin

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name niacin
Generic Name niacin
Labeler lannett company, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

niacin 1000 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 62175-322
Product ID 62175-322_7e9530d1-a940-42e8-b754-0d4089b39db1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203899
Listing Expiration 2026-12-31
Marketing Start 2017-02-16

Pharmacologic Class

Established (EPC)
nicotinic acid [epc]
Chemical Structure
nicotinic acids [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62175322
Hyphenated Format 62175-322

Supplemental Identifiers

RxCUI
1098134 1098141
UPC
0362175320469
UNII
2679MF687A
NUI
N0000175594 M0014839

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 niacin (source: ndc)
Generic Name niacin (source: ndc)
Application Number ANDA203899 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-43)
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-46)
source: ndc

Packages (2)

62175-322-43 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-43) 62175-322-46 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-46)

Ingredients (1)

niacin (1000 mg/1)

Linked Drug Pages (1)

Niacin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7e9530d1-a940-42e8-b754-0d4089b39db1", "openfda": {"nui": ["N0000175594", "M0014839"], "upc": ["0362175320469"], "unii": ["2679MF687A"], "rxcui": ["1098134", "1098141"], "spl_set_id": ["d7b66e13-00ed-48a9-a54a-8e474cc31d54"], "pharm_class_cs": ["Nicotinic Acids [CS]"], "pharm_class_epc": ["Nicotinic Acid [EPC]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-43)", "package_ndc": "62175-322-43", "marketing_start_date": "20170216"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-322-46)", "package_ndc": "62175-322-46", "marketing_start_date": "20170216"}], "brand_name": "Niacin", "product_id": "62175-322_7e9530d1-a940-42e8-b754-0d4089b39db1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Nicotinic Acid [EPC]", "Nicotinic Acids [CS]"], "product_ndc": "62175-322", "generic_name": "Niacin", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Niacin", "active_ingredients": [{"name": "NIACIN", "strength": "1000 mg/1"}], "application_number": "ANDA203899", "marketing_category": "ANDA", "marketing_start_date": "20170216", "listing_expiration_date": "20261231"}