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: 65841-024_f4fb6b85-6379-4e8a-9ee3-402819d128a0
Product NDC: 65841-024
Form: TABLET
Composition / generic term: Atenolol
Labeler: Zydus Lifesciences Limited
Marketing category: ANDA
Marketing start / end (source format): 20051008
Source listing expiry: 20261231

Source-listed ingredients

ATENOLOL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (65841-024-01) · 65841-024-01
1000 TABLET in 1 BOTTLE (65841-024-10) · 65841-024-10
90 TABLET in 1 BOTTLE (65841-024-16) · 65841-024-16
5000 TABLET in 1 BOTTLE (65841-024-40) · 65841-024-40

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.

Browse United States records →