Propafenone Hydrochloride
NDC 60687-709, Propafenone Hydrochloride, tablet, film coated, from American Health Packaging.
- Product NDC
- 60687-709
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075938
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60687-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROPAFENONE HYDROCHLORIDE150 mg/1
Pharmacologic classes
Antiarrhythmic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-709-01 | 60687070901 | 100 BLISTER PACK in 1 CARTON (60687-709-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-709-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/343e4ad7-05e2-4e6c-8f8e-91c07739cae2NADAC price for package 60687070901
GET /v1/drugs/nadac/60687070901
Use it
Look up 60687-709 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-709 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-709. 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.