Digoxin
NDC 70954-201, Digoxin, tablet, from ANI Pharmaceuticals, Inc..
- Product NDC
- 70954-201
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215307
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70954-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DIGOXIN.125 mg/1
Pharmacologic classes
Cardiac Glycoside [EPC]; Cardiac Glycosides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70954-201-10 | 70954020110 | 100 TABLET in 1 BOTTLE (70954-201-10) |
| 70954-201-20 | 70954020120 | 1000 TABLET in 1 BOTTLE (70954-201-20) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dba3b3f7-3ff2-4996-8653-b0e54a398bf9NADAC price for package 70954020110
GET /v1/drugs/nadac/70954020110NADAC price for package 70954020120
GET /v1/drugs/nadac/70954020120
Use it
Look up 70954-201 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70954-201 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70954-201. 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.