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Nebivolol

NDC 71209-058, Nebivolol, tablet, from Cadila Pharmaceuticals Limited.

Product NDC
71209-058
Status
Listed
Labeler
Cadila Pharmaceuticals Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208717
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71209-058 \
  -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
71209-058-017120900580130 TABLET in 1 BOTTLE (71209-058-01)
71209-058-047120900580490 TABLET in 1 BOTTLE (71209-058-04)
71209-058-0571209005805100 TABLET in 1 BOTTLE (71209-058-05)
71209-058-11712090058111000 TABLET in 1 BOTTLE (71209-058-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/451cdd6e-13b4-402f-8a44-cdf5f7433a49

Use it

Look up 71209-058 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71209-058 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71209-058. 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.