Levothyroxine Sodium
- Product NDC
- 50090-5887
- 11-digit product format
- 500905887
- Labeler code
- 50090
- Product ID
- 50090-5887_092a8136-cec6-4281-b475-c1618254638c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-08-03
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 175 ug/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5887 | LEVOTHYROXINE SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC | 20220104_96ff9cec-6047-4e9e-afb4-cab91b4abcca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5887-0 | 50090588700 | 30 TABLET in 1 BOTTLE (50090-5887-0) | 30 tablet | 2021-12-29 | 0000-00-00 | No | No | Current |
| 50090-5887-1 | 50090588701 | 90 TABLET in 1 BOTTLE (50090-5887-1) | 90 tablet | 2021-12-29 | 0000-00-00 | No | No | Current |