Midodrine Hydrochloride
NDC 59651-247, Midodrine Hydrochloride, tablet, from Aurobindo Pharma Limited.
- Product NDC
- 59651-247
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212774
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-247 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MIDODRINE HYDROCHLORIDE5 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-247-01 | 59651024701 | 1 BOTTLE in 1 CARTON (59651-247-01) / 100 TABLET in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/771b3e81-f15b-4d32-a1d8-c43b104d1f7bNADAC price for package 59651024701
GET /v1/drugs/nadac/59651024701
Use it
Look up 59651-247 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-247 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-247. 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.