Mexiletine Hydrochloride
NDC 62559-821, Mexiletine Hydrochloride, capsule, from ANI Pharmaceuticals, Inc..
- Product NDC
- 62559-821
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA074450
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/62559-821 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MEXILETINE HYDROCHLORIDE200 mg/1
Pharmacologic classes
Antiarrhythmic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 62559-821-01 | 62559082101 | 100 CAPSULE in 1 BOTTLE (62559-821-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1b3a807f-368a-42dc-8266-ddf8347a8826NADAC price for package 62559082101
GET /v1/drugs/nadac/62559082101
Use it
Look up 62559-821 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62559-821 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62559-821. 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.