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Nebivolol

NDC 59651-137, Nebivolol, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-137
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211053
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-137 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NEBIVOLOL HYDROCHLORIDE2.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
59651-137-305965101373030 TABLET in 1 BOTTLE (59651-137-30)
59651-137-905965101379090 TABLET in 1 BOTTLE (59651-137-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e43a4e2-574e-4f4a-804d-e346b4edd2f1

  • NADAC price for package 59651013730

    GET /v1/drugs/nadac/59651013730

Use it

Look up 59651-137 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-137 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-137. 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.