Liothyronine Sodium
- Product NDC
- 75907-004
- 11-digit product format
- 759070004
- Labeler code
- 75907
- Product ID
- 75907-004_284a71c7-5913-ff21-9733-f0cf9fc379c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dr. Reddy's Labratories Inc.
- Application
- ANDA090097
- Marketing category
- ANDA
- Marketing start
- 2024-03-15
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 50 ug/1
- Pharmacologic classes
- Triiodothyronine [CS], l-Triiodothyronine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Liothyronine Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIOTHYRONINE SODIUM | 50 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | GCA9VV7D2N |
| Rxcui | 903456, 903697, 903703 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 75907-004-01 | Liothyronine Sodium | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75907-004 | LIOTHYRONINE SODIUM TABLET [DR. REDDY'S LABRATORIES INC.] | 1 | Current NDC, 1 package rows | 20240316_0b0f2db9-642d-d84f-b102-b43de34bbe75.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 |
|---|
| 75907-004-01 | 75907000401 | 100 TABLET in 1 BOTTLE, PLASTIC (75907-004-01) | 100 tablet | 2024-03-15 | No | No | Current |