levothyroxine sodium
- Product NDC
- 50090-4899
- 11-digit product format
- 500904899
- Labeler code
- 50090
- Product ID
- 50090-4899_7761e7dc-6c3b-4c9c-8b50-96c45999a7a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021116
- Marketing category
- NDA
- Marketing start
- 2019-05-07
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 75 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4899-0 | levothyroxine sodium | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4899 | LEVOTHYROXINE SODIUM TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20210303_eceefcf0-d2a3-4661-86b2-046ed8ded836.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4899-0 | 50090489900 | 90 TABLET in 1 BOTTLE (50090-4899-0) | 90 tablet | 2020-02-14 | 0000-00-00 | No | No | Current |