United States · FDA National Drug Code directory

TENORMIN

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
52427-430_ecd0de7b-801e-a5d6-01b7-01b89a8f3a78
Product NDC
52427-430
Form
TABLET
Composition / generic term
Atenolol
Labeler
Almatica Pharma LLC
Marketing category
NDA
Marketing start / end (source format)
20150415 / 20260930

Source-listed ingredients

  • ATENOLOL — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (52427-430-90) · 52427-430-90

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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