Levothyroxine Sodium
- Product NDC
- 43063-191
- 11-digit product format
- 430630191
- Labeler code
- 43063
- Product ID
- 43063-191_785ad0af-b94e-98af-e053-2991aa0adfaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA021210
- Marketing category
- NDA
- Marketing start
- 2003-12-01
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 0 mg/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