Levothyroxine sodium
- Product NDC
- 35356-955
- 11-digit product format
- 353560955
- Labeler code
- 35356
- Product ID
- 35356-955_78a603d7-65a7-4560-9a34-6050f309e370
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- NDA021342
- Marketing category
- NDA
- Marketing start
- 2002-03-01
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 88 ug/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record