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Niacor

NDC 71740-001, Niacin, tablet, from Avondale Pharmaceuticals, LLC.

Product NDC
71740-001
Status
Listed
Labeler
Avondale Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040378
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71740-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIACIN500 mg/1

Pharmacologic classes

Nicotinic Acid [EPC]; Nicotinic Acids [CS]

Package NDCNDC-11Package
71740-001-1071740000110100 TABLET in 1 BOTTLE (71740-001-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bf287412-160b-403f-8eb4-57f29a475902

Use it

Look up 71740-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71740-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71740-001. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.