Liothyronine Sodium
NDC 71335-0166, Liothyronine Sodium, tablet, from Bryant Ranch Prepack.
- Product NDC
- 71335-0166
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200295
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0166 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LIOTHYRONINE SODIUM25 ug/1
Pharmacologic classes
Triiodothyronine [CS]; l-Triiodothyronine [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71335-0166-1 | 71335016601 | 30 TABLET in 1 BOTTLE (71335-0166-1) |
| 71335-0166-2 | 71335016602 | 28 TABLET in 1 BOTTLE (71335-0166-2) |
| 71335-0166-3 | 71335016603 | 60 TABLET in 1 BOTTLE (71335-0166-3) |
| 71335-0166-4 | 71335016604 | 100 TABLET in 1 BOTTLE (71335-0166-4) |
| 71335-0166-5 | 71335016605 | 90 TABLET in 1 BOTTLE (71335-0166-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7efdd16d-37e6-4dc8-a6c5-5b42c4813379
Use it
Look up 71335-0166 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0166 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0166. 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.