Levothyroxine sodium
NDC 71205-642, Levothyroxine Sodium, tablet, from Proficient Rx LP.
- Product NDC
- 71205-642
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212399
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-642 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOTHYROXINE SODIUM100 ug/1
Pharmacologic classes
Thyroxine [CS]; l-Thyroxine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-642-30 | 71205064230 | 30 TABLET in 1 BOTTLE (71205-642-30) |
| 71205-642-60 | 71205064260 | 60 TABLET in 1 BOTTLE (71205-642-60) |
| 71205-642-90 | 71205064290 | 90 TABLET in 1 BOTTLE (71205-642-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9d1aaa2d-c8c0-478f-8540-f92f6512cfcb
Use it
Look up 71205-642 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-642 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-642. 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.