Levothyroxine sodium
- Product NDC
- 68071-4624
- 11-digit product format
- 680714624
- Labeler code
- 68071
- Product ID
- 68071-4624_bdb04124-d671-2b99-e053-2995a90ab2aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2002-03-01
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 50 ug/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4624-3 | 68071462403 | 30 TABLET in 1 BOTTLE (68071-4624-3) | 30 tablet | 2018-11-12 | 0000-00-00 | No | No | Current |
| 68071-4624-9 | 68071462409 | 90 TABLET in 1 BOTTLE (68071-4624-9) | 90 tablet | 2018-11-12 | 0000-00-00 | No | No | Current |