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NADOLOL

NDC 71335-3127, NADOLOL, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3127
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211763
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3127 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NADOLOL80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-3127-17133531270130 TABLET in 1 BOTTLE (71335-3127-1)
71335-3127-27133531270228 TABLET in 1 BOTTLE (71335-3127-2)
71335-3127-37133531270390 TABLET in 1 BOTTLE (71335-3127-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/64a788d0-b7f0-4f39-8adb-ab68870ecfa5

Use it

Look up 71335-3127 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3127 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3127. 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.