United States · FDA National Drug Code directory

Atenolol

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
50090-7603_3623803e-071f-459c-804e-58b8af884727
Product NDC
50090-7603
Form
TABLET
Composition / generic term
Atenolol
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20191121
Source listing expiry
20261231

Source-listed ingredients

  • ATENOLOL — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (50090-7603-0) · 50090-7603-0

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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