NIACIN
- Product NDC
- 68084-756
- 11-digit product format
- 680840756
- Labeler code
- 68084
- Product ID
- 68084-756_d100729c-fa82-481e-e053-2995a90afc46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIACIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA090860
- Marketing category
- ANDA
- Marketing start
- 2014-05-08
- Marketing end
- 2022-03-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-756-35 | 68084075635 | 60 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-756-35) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-756-95) | 60 blister pack | 2014-05-08 | 0000-00-00 | No | No | Current |