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
- 47335-613_bc18daa3-5321-43bd-9d00-dabd9adac571
- Product NDC
- 47335-613
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- NIACIN
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140627
- Source listing expiry
- 20261231
Source-listed ingredients
- NIACIN — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-08) · 47335-613-08
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-18) · 47335-613-18
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-81) · 47335-613-81
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-83) · 47335-613-83
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-88) · 47335-613-88
Source and coverage
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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.
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