Liothyronine Sodium
- Product NDC
- 63629-6540
- 11-digit product format
- 636296540
- Labeler code
- 63629
- Product ID
- 63629-6540_7331dbd3-c64a-4ac5-988a-f65b72bb07b8
- 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
- 5 ug/1
- Pharmacologic classes
- l-Triiodothyronine [EPC],Triiodothyronine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record