Propranolol Hydrochloride ER
NDC 62559-530, propranolol hydrochloride, capsule, extended release, from ANI Pharmaceuticals, Inc..
- Product NDC
- 62559-530
- Status
- Listed
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA018553
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/62559-530 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROPRANOLOL HYDROCHLORIDE60 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 62559-530-01 | 62559053001 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-530-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5415904b-90da-48e8-9f9e-f86749aa129c
Use it
Look up 62559-530 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62559-530 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62559-530. 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.