Levothyroxine Sodium
NDC 67046-0569, Levothyroxine Sodium, tablet, from Coupler LLC.
- Product NDC
- 67046-0569
- Status
- Listed
- Labeler
- Coupler LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209713
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0569 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOTHYROXINE SODIUM.1 mg/1
Pharmacologic classes
Thyroxine [CS]; l-Thyroxine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 67046-0569-3 | 67046056903 | 30 TABLET in 1 BLISTER PACK (67046-0569-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/52cce695-4363-8a2c-e063-6294a90a1bbf
Use it
Look up 67046-0569 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67046-0569 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67046-0569. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.