Levothyroxine sodium
- Product NDC
- 0781-5191
- 11-digit product format
- 007815191
- Labeler code
- 0781
- Product ID
- 0781-5191_b6216747-5ffb-6cd7-e053-2995a90a5ca0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sandoz Inc.
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2002-03-01
- Marketing end
- 2021-12-31
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 137 ug/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-5191-10 | 00781519110 | 1000 TABLET in 1 BOTTLE (0781-5191-10) | 1000 tablet | 2002-03-01 | 2021-12-31 | No | No | Current |
| 0781-5191-92 | 00781519192 | 90 TABLET in 1 BOTTLE (0781-5191-92) | 90 tablet | 2012-04-16 | 2021-12-31 | No | No | Current |