Levothyroxine sodium
NDC 70518-4396, Levothyroxine Sodium, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-4396
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- 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/70518-4396 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOTHYROXINE SODIUM112 ug/1
Pharmacologic classes
Thyroxine [CS]; l-Thyroxine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4396-0 | 70518439600 | 90 TABLET in 1 BOTTLE (70518-4396-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/0fa2e2f5-401b-45c1-b6a5-d02f6faf509d
Use it
Look up 70518-4396 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4396 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4396. 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.