Niacin 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

NDC 1147335-0539-88
Product NDC47335-0539
Generic Drug NameNiacin
Brand NameNiacin
ManufacturerSun Pharmaceutical Industries, Inc.
Strength500 mg / 1
Dosage FormTablet
Drug TypeOral
Package Quantity100 Tablet, Film Coated, Extended Release
Package Description100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-88)
Active IngredientsNiacin
Marketing CategoryANDA

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NDC snapshot

Niacin 500 mg / 1 Tablet is tracked under NDC 47335-0539-88 and rolls up into product family 47335-0539. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

  • Package configuration: 100 Tablet, Film Coated, Extended Release.
  • Manufacturer: Sun Pharmaceutical Industries, Inc..
  • Dosage form: Tablet.
  • Family size: 5 indexed presentations.

Official references

Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.

Alternate presentations in this family

These nearby package-level pages can help healthcare teams compare related packaging or presentation differences inside the same product-NDC family.

Niacin 500 mg / 1 Tablet 100 Tablet, Film Coated, Extended Release, NDC 47335-0539-88, is a Sun Pharmaceutical Industries, Inc. 500 mg / 1 tablet presentation packaged as 100 Tablet, Film Coated, Extended Release.

NDC search formats

  • Canonical NDC 11: 47335-0539-88
  • Digits-only NDC 11: 47335053988
  • Possible 10-digit display format: 47335-539-88 (4733553988)

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