Sotalol Hydrochloride
NDC 0093-1060, Sotalol Hydrochloride, tablet, from Teva Pharmaceuticals USA, Inc..
- Product NDC
- 0093-1060
- Status
- Listed
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075429
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0093-1060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SOTALOL HYDROCHLORIDE120 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; Antiarrhythmic [EPC]; Cardiac Rhythm Alteration [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0093-1060-01 | 00093106001 | 100 TABLET in 1 BOTTLE (0093-1060-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8e2772cb-7dea-42d1-ba31-d479ba7cb09aNADAC price for package 00093106001
GET /v1/drugs/nadac/00093106001
Use it
Look up 0093-1060 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0093-1060 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0093-1060. 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.