Niacor
- Product NDC
- 71740-201
- 11-digit product format
- 717400201
- Labeler code
- 71740
- Product ID
- 71740-201_2088558c-8be0-47ba-8bbf-fbf26088c0ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- niacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Avondale Pharmaceuticals, LLC
- Application
- ANDA040378
- Marketing category
- ANDA
- Marketing start
- 2000-05-03
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71740-201-10 | 71740020110 | 100 TABLET in 1 BOTTLE (71740-201-10) | 100 tablet | 2017-11-13 | 0000-00-00 | No | No | Current |