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
- 69452-172_4526a56d-6695-5338-e063-6294a90aa2b0
- Product NDC
- 69452-172
- 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 — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (69452-172-13) · 69452-172-13
- 3 BLISTER PACK in 1 CARTON (69452-172-72) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 69452-172-72
- 1 BLISTER PACK in 1 CARTON (69452-172-74) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 69452-172-74
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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