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Niacin

NDC 65162-322, Niacin, tablet, film coated, extended release, from Amneal Pharmaceuticals LLC.

Product NDC
65162-322
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204178
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NIACIN750 mg/1

Pharmacologic classes

Nicotinic Acid [EPC]; Nicotinic Acids [CS]

Package NDCNDC-11Package
65162-322-036516203220330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-03)
65162-322-096516203220990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-09)
65162-322-5065162032250500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65162-322-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7250313b-b2ef-4736-bd25-2f29c2ac0eb9

Use it

Look up 65162-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-322. 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.