United States · FDA National Drug Code directory

Azithromycin

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: 69452-171_4526a56d-6695-5338-e063-6294a90aa2b0
Product NDC: 69452-171
Form: TABLET, FILM COATED
Composition / generic term: Azithromycin
Labeler: Bionpharma Inc.
Marketing category: ANDA
Marketing start / end (source format): 20190312
Source listing expiry: 20261231

Source-listed ingredients

AZITHROMYCIN DIHYDRATE — 250 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BLISTER PACK in 1 CARTON (69452-171-04) / 6 TABLET, FILM COATED in 1 BLISTER PACK · 69452-171-04
30 TABLET, FILM COATED in 1 BOTTLE (69452-171-13) · 69452-171-13
3 BLISTER PACK in 1 CARTON (69452-171-73) / 6 TABLET, FILM COATED in 1 BLISTER PACK · 69452-171-73

Source and coverage

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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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