MIDODRINE HYDROCHLORIDE
NDC 46708-339, MIDODRINE HYDROCHLORIDE, tablet, from Alembic Pharmaceuticals Limited.
- Product NDC
- 46708-339
- Status
- Listed
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214734
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/46708-339 \ -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 |
|---|---|---|
| 46708-339-31 | 46708033931 | 100 TABLET in 1 BOTTLE (46708-339-31) |
| 46708-339-71 | 46708033971 | 500 TABLET in 1 BOTTLE (46708-339-71) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/03b54024-2a26-4abe-bd8b-b66bb6781fa7
Use it
Look up 46708-339 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/46708-339 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 46708-339. 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.