Levothyroxine Sodium
NDC 71335-2290, Levothyroxine Sodium, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-2290
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA021342
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2290 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOTHYROXINE SODIUM88 ug/1
Pharmacologic classes
Thyroxine [CS]; l-Thyroxine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-2290-1 | 71335229001 | 1000 TABLET in 1 BOTTLE (71335-2290-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e293dd94-b523-47a2-8bed-e6d99945ee59
Use it
Look up 71335-2290 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2290 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-2290. 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.