NIACIN
- Product NDC
- 51407-118
- 11-digit product format
- 514070118
- Labeler code
- 51407
- Product ID
- 51407-118_b2c022ec-030f-5f32-e053-2a95a90a51bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIACIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA090446
- Marketing category
- ANDA
- Marketing start
- 2014-03-20
- Marketing end
- 0000-00-00
- Substance
- NIACIN
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Nicotinic Acid [EPC],Nicotinic Acids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 51407-118-90 | 51407011890 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (51407-118-90) | 2018-06-07 | 0000-00-00 | No | No | Current |