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Nadolol

NDC 68001-690, Nadolol, tablet, from BluePoint Laboratories.

Product NDC
68001-690
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201893
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-690 \
  -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
68001-690-0068001069000100 TABLET in 1 BOTTLE (68001-690-00)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f11553f1-18ec-41b0-a7ad-1c9f21ef2c9f

  • NADAC price for package 68001069000

    GET /v1/drugs/nadac/68001069000

Use it

Look up 68001-690 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-690 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-690. 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.