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
- 72189-088_4d3a98e6-31e9-c271-e063-6394a90aa19e
- Product NDC
- 72189-088
- Form
- TABLET, FILM COATED
- Composition / generic term
- AZITHROMYCIN
- Labeler
- DIRECT RX
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200618
- Source listing expiry
- 20271231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE (72189-088-02) · 72189-088-02
- 3 TABLET, FILM COATED in 1 BOTTLE (72189-088-03) · 72189-088-03
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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