Niacin 47335-0613
Product NDC
47335-0613- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 27, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA200484
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Niacin | 1000 mg/1 |
Drug Class
Nicotinic Acid [EPC]Nicotinic Acid [EPC]Nicotinic Acids [CS]
Packaging Options(5)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-08)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-18)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-81)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-83)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-613-88)