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ivabradine

NDC 69452-191, ivabradine, tablet, film coated, from Bionpharma Inc..

Product NDC
69452-191
Status
Listed
Labeler
Bionpharma Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213276
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69452-191 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IVABRADINE HYDROCHLORIDE7.5 mg/1

Pharmacologic classes

Hyperpolarization-activated Cyclic Nucleotide-gated Channel Antagonists [MoA]; Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker [EPC]

Package NDCNDC-11Package
69452-191-176945201911760 TABLET, FILM COATED in 1 BOTTLE (69452-191-17)
69452-191-3069452019130500 TABLET, FILM COATED in 1 BOTTLE (69452-191-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ead1cf3-e61a-49c4-e063-6294a90a330f

  • NADAC price for package 69452019117

    GET /v1/drugs/nadac/69452019117

Use it

Look up 69452-191 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69452-191 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69452-191. 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.