Sotalol Hydrochloride
NDC 60505-0082, Sotalol Hydrochloride, tablet, from Apotex Corp..
- Product NDC
- 60505-0082
- Status
- Listed
- Labeler
- Apotex Corp.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076140
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60505-0082 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SOTALOL HYDROCHLORIDE240 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; Antiarrhythmic [EPC]; Cardiac Rhythm Alteration [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60505-0082-0 | 60505008200 | 100 TABLET in 1 BOTTLE (60505-0082-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1a56c82e-7ecd-43b0-2899-f89e47adf7dbNADAC price for package 60505008200
GET /v1/drugs/nadac/60505008200
Use it
Look up 60505-0082 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60505-0082 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60505-0082. 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.