Liothyronine Sodium
- Product NDC
- 43063-253
- 11-digit product format
- 430630253
- Labeler code
- 43063
- Product ID
- 43063-253_80c70a43-9ba8-92af-e053-2991aa0abc7e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, In
- Application
- ANDA090097
- Marketing category
- ANDA
- Marketing start
- 2009-03-23
- Marketing end
- 2019-09-01
- Substance
- LIOTHYRONINE SO
- Active strength
- 25 ug/1
- Pharmacologic classes
- l-Triiodothyron
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record