Levothyroxine Sodium
- Product NDC
- 82804-099
- 11-digit product format
- 828040099
- Labeler code
- 82804
- Product ID
- 82804-099_9e69af45-d5a3-4986-8ea5-dee9e59272d7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-08-03
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 50 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 | 50 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 966221 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82804-099-30 | Levothyroxine Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 82804-099-90 | 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 |
|---|
| 82804-099 | LEVOTHYROXINE SODIUM TABLET [PROFICIENT RX LP] | 2 | Current NDC, 2 package rows | 20240522_e1b322a6-9161-45b9-bf77-3c44502d5efd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-099-30 | 82804009930 | 30 TABLET in 1 BOTTLE (82804-099-30) | 30 tablet | 2024-04-25 | No | No | Current |
| 82804-099-90 | 82804009990 | 90 TABLET in 1 BOTTLE (82804-099-90) | 90 tablet | 2024-05-01 | No | No | Current |