LEVOTHYROXINE SODIUM
- Product NDC
- 72189-155
- 11-digit product format
- 721890155
- Labeler code
- 72189
- Product ID
- 72189-155_1922dbd9-96de-8652-e063-6294a90a0afe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- NDA021116
- Marketing category
- NDA
- Marketing start
- 2020-12-01
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9J765S329G | LEVOTHYROXINE SODIUM | 6106-07-6 | LEVOTHYROXINE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-155-30 | 72189015530 | 30 TABLET in 1 BOTTLE (72189-155-30) | 30 tablet | 2020-12-01 | No | No | Historical |
| 72189-155-90 | 72189015590 | 90 TABLET in 1 BOTTLE (72189-155-90) | 90 tablet | 2020-12-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LEVOTHYROXINE SODIUM | DIRECT RX | 2024-05-23 | HUMAN PRESCRIPTION DRUG LABEL | 21 |