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nebivolol

NDC 68462-618, nebivolol hydrochloride, tablet, from Glenmark Pharmaceuticals Inc., USA.

Product NDC
68462-618
Status
Listed
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203821
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-618 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NEBIVOLOL HYDROCHLORIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68462-618-0168462061801100 TABLET in 1 BOTTLE (68462-618-01)
68462-618-116846206181110 BLISTER PACK in 1 CARTON (68462-618-11) / 10 TABLET in 1 BLISTER PACK
68462-618-306846206183030 TABLET in 1 BOTTLE (68462-618-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cb47560d-9e35-4b0f-b12b-6ea478684a5b

Use it

Look up 68462-618 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-618 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-618. 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.