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Propranolol Hydrochloride ER

NDC 62559-532, propranolol hydrochloride, capsule, extended release, from ANI Pharmaceuticals, Inc..

Product NDC
62559-532
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
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62559-532 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROPRANOLOL HYDROCHLORIDE120 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
62559-532-0162559053201100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62559-532-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5415904b-90da-48e8-9f9e-f86749aa129c

Use it

Look up 62559-532 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62559-532 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62559-532. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.