Levothyroxine Sodium
- Product NDC
- 68071-4731
- 11-digit product format
- 680714731
- Labeler code
- 68071
- Product ID
- 68071-4731_c0567f5c-f9d0-88d9-e053-2995a90a624a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare 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
- 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 |
|---|
| 68071-4731-3 | 68071473103 | 30 TABLET in 1 BOTTLE (68071-4731-3) | 30 tablet | 2019-01-23 | 0000-00-00 | No | No | Current |