LEVOTHYROXINE SODIUM
- Product NDC
- 72189-346
- 11-digit product format
- 721890346
- Labeler code
- 72189
- Product ID
- 72189-346_2c4c7c58-18dd-4126-e063-6294a90aff5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2022-04-19
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 200 ug/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LEVOTHYROXINE SODIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LEVOTHYROXINE SODIUM | 200 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 892251 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-346-90 | LEVOTHYROXINE SODIUM | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-346 | LEVOTHYROXINE SODIUM TABLET [DIRECT RX] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250123_dd032289-acee-49fc-e053-2a95a90a5999.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 |
|---|
| 72189-346-90 | 72189034690 | 90 TABLET in 1 BOTTLE (72189-346-90) | 90 tablet | 2022-04-19 | 0000-00-00 | No | No | Current |