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NEBIVOLOL

NDC 71335-3102, NEBIVOLOL, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3102
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217397
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NEBIVOLOL HYDROCHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-3102-17133531020130 TABLET in 1 BOTTLE (71335-3102-1)
71335-3102-27133531020290 TABLET in 1 BOTTLE (71335-3102-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aad20a92-bc2e-4624-b588-c6d40facd3a7

Use it

Look up 71335-3102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3102. 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.