NDC 47335-539 – Niacin
Niacin 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC47335-539
Product details
- Brand name
- Niacin
- Generic name
- Niacin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA200484
- Marketed since
- June 27, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nicotinic Acid
Active ingredients
- Niacin 500 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 47335-539-08 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-08) | Jun 27, 2014 |
| 47335-539-18 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-18) | Jun 27, 2014 |
| 47335-539-81 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-81) | Jun 27, 2014 |
| 47335-539-83 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-83) | Jun 27, 2014 |
| 47335-539-88 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-539-88) | Jun 27, 2014 |
Recalls mentioning this NDC
- D-0270-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment. - D-0269-2024 Jan 31, 2024 · Class II
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
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