liothyronine sodium
- Product NDC
- 63629-8337
- 11-digit product format
- 636298337
- Labeler code
- 63629
- Product ID
- 63629-8337_387b6eb3-9d31-49d5-a6c3-994abc5fbd9e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- liothyronine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA091382
- Marketing category
- ANDA
- Marketing start
- 2019-11-28
- Marketing end
- 0000-00-00
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 50 ug/1
- Pharmacologic classes
- Triiodothyronine [CS], l-Triiodothyronine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| GCA9VV7D2N | LIOTHYRONINE SODIUM | 55-06-1 | LIOTHYRONINE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8337-1 | 63629833701 | 30 TABLET in 1 BOTTLE (63629-8337-1) | 30 tablet | 2020-07-17 | 0000-00-00 | No | No | Current |