NIACIN
- Product NDC
- 68084-773
- 11-digit product format
- 680840773
- Labeler code
- 68084
- Product ID
- 68084-773_75b26af4-19fb-cf08-e053-2991aa0a556d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIACIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA090446
- Marketing category
- ANDA
- Marketing start
- 2014-09-25
- Marketing end
- 2019-05-31
- Substance
- NIACIN
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Nicotinic Acid [EPC],Nicotinic Acids [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record