Liothyronine Sodium
- Product NDC
- 63629-8154
- 11-digit product format
- 636298154
- Labeler code
- 63629
- Product ID
- 63629-8154_ab626baa-29f7-46c1-bf29-9e8037e5dd93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200295
- Marketing category
- ANDA
- Marketing start
- 2012-12-03
- Marketing end
- 0000-00-00
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 50 ug/1
- Pharmacologic classes
- l-Triiodothyronine [EPC],Triiodothyronine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 63629-8154-1 | 63629815401 | 30 TABLET in 1 BOTTLE (63629-8154-1) | 30 tablet | 2012-12-03 | 0000-00-00 | No | No | Current |
| 63629-8154-2 | 63629815402 | 60 TABLET in 1 BOTTLE (63629-8154-2) | 60 tablet | 2019-06-25 | 0000-00-00 | No | No | Current |