United States · FDA National Drug Code directory

NIACIN

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 68180-222_309a40e8-333f-478a-8a94-beff7f3ca5b2
Product NDC: 68180-222
Form: TABLET, EXTENDED RELEASE
Composition / generic term: NIACIN
Labeler: Lupin Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20140320
Source listing expiry: 20261231

Source-listed ingredients

NIACIN — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →