Levothyroxine sodium
- Product NDC
- 82804-149
- 11-digit product format
- 828040149
- Labeler code
- 82804
- Product ID
- 82804-149_b4f8dfd0-b15a-4da5-a0d0-ad768e0b7ff8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA207588
- Marketing category
- ANDA
- Marketing start
- 2022-09-21
- 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 |
|---|
| 82804-149-30 | 82804014930 | 30 TABLET in 1 BOTTLE (82804-149-30) | 30 tablet | 2024-09-20 | No | No | Historical |
| 82804-149-90 | 82804014990 | 90 TABLET in 1 BOTTLE (82804-149-90) | 90 tablet | 2024-09-20 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Proficient Rx LP | 2024-09-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |