NIACIN
- Product NDC
- 63629-7193
- 11-digit product format
- 636297193
- Labeler code
- 63629
- Product ID
- 63629-7193_be49adf4-7469-44a8-b92a-3e20f05a808e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NIACIN
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090860
- Marketing category
- ANDA
- Marketing start
- 2014-03-20
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7193-1 | 63629719301 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-7193-1) | 2017-02-28 | 0000-00-00 | No | No | Current |