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NADOLOL

NDC 72664-211, NADOLOL, tablet, from VGYAAN Pharmaceuticals LLC.

Product NDC
72664-211
Status
Listed
Labeler
VGYAAN Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212856
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72664-211 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NADOLOL20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72664-211-0172664021101100 TABLET in 1 BOTTLE, PLASTIC (72664-211-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/85b4b931-51c4-4326-88ea-708dde8323d4

Use it

Look up 72664-211 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72664-211 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72664-211. 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.