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Nebivolol

NDC 70756-292, Nebivolol, tablet, from Lifestar Pharma LLC.

Product NDC
70756-292
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216172
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-292 \
  -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
70756-292-307075602923030 TABLET in 1 BOTTLE (70756-292-30)
70756-292-907075602929090 TABLET in 1 BOTTLE (70756-292-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2639abce-a5ca-4b7f-99d7-026ab3233aaa

Use it

Look up 70756-292 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-292 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-292. 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.