Midodrine Hydrochloride
NDC 72162-1975, midodrine hydrochloride, tablet, from Bryant Ranch Prepack.
- Product NDC
- 72162-1975
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207849
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1975 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MIDODRINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA]; alpha-Adrenergic Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72162-1975-1 | 72162197501 | 100 TABLET in 1 BOTTLE, PLASTIC (72162-1975-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/78446de1-81f6-4764-98f3-44b4057f2175
Use it
Look up 72162-1975 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1975 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-1975. 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.