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NADOLOL

NDC 46708-402, NADOLOL, tablet, from Alembic Pharmaceuticals Limited.

Product NDC
46708-402
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
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/46708-402 \
  -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
46708-402-304670804023030 TABLET in 1 BOTTLE (46708-402-30)
46708-402-3146708040231100 TABLET in 1 BOTTLE (46708-402-31)
46708-402-91467080402911000 TABLET in 1 BOTTLE (46708-402-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0bd202e3-c673-4945-b828-1a5bc6a896ae

Use it

Look up 46708-402 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-402 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-402. 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.