Niaspan
- Product NDC
- 50090-1536
- 11-digit product format
- 500901536
- Labeler code
- 50090
- Product ID
- 50090-1536_b76b2949-6f4b-4d6e-ae7e-cac16c0dd779
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Niacin
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA020381
- Marketing category
- NDA
- Marketing start
- 2010-06-29
- Marketing end
- 0000-00-00
- Substance
- NIACIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Nicotinic Acid [EPC],Nicotinic Acids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record