SOTALOL HYDROCHLORIDE
NDC 59651-775, SOTALOL HYDROCHLORIDE, tablet, from Aurobindo Pharma Limited.
- Product NDC
- 59651-775
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077616
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-775 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SOTALOL HYDROCHLORIDE80 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; Antiarrhythmic [EPC]; Cardiac Rhythm Alteration [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-775-01 | 59651077501 | 100 TABLET in 1 BOTTLE (59651-775-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/6f3145d7-f3c9-4456-a77d-d04c54f24668NADAC price for package 59651077501
GET /v1/drugs/nadac/59651077501
Use it
Look up 59651-775 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-775 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-775. 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.