Levothyroxine Sodium
NDC 72162-1095, Levothyroxine Sodium, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-1095
- 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/72162-1095 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LEVOTHYROXINE SODIUM300 ug/1
Pharmacologic classes
Thyroxine [CS]; l-Thyroxine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1095-0 | 72162109500 | 1000 TABLET in 1 BOTTLE (72162-1095-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d0beda93-9454-4846-b5c6-2a9113fb1765
Use it
Look up 72162-1095 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1095 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1095. 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.