Niaspan
- Product NDC
- 0074-3265
- 11-digit product format
- 000743265
- Labeler code
- 0074
- Product ID
- 0074-3265_4d0c980a-6f82-417b-ad85-ff1561bb1f4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Niacin
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AbbVie Inc.
- Application
- NDA020381
- Marketing category
- NDA
- Marketing start
- 2017-09-19
- Marketing end
- 2022-08-02
- Substance
- NIACIN
- Active strength
- 500 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0074-3265-90 | 00074326590 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-3265-90) | 2017-09-19 | 0000-00-00 | No | No | Current |