Liothyronine Sodium
- Product NDC
- 63629-6391
- 11-digit product format
- 636296391
- Labeler code
- 63629
- Product ID
- 63629-6391_b6d164bc-633a-4e49-a165-0faeb9a5ae7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200295
- Marketing category
- ANDA
- Marketing start
- 2012-11-30
- Marketing end
- 0000-00-00
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 25 ug/1
- Pharmacologic classes
- l-Triiodothyronine [EPC],Triiodothyronine [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 |
|---|
| 63629-6391-1 | 63629639101 | 30 TABLET in 1 BOTTLE (63629-6391-1) | 30 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |