United States · FDA National Drug Code directory
Azithromycin Dihydrate
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
- 51224-122_4e2d2728-b3ae-4a85-8c2a-5e74c60a0f6b
- Product NDC
- 51224-122
- Form
- TABLET, FILM COATED
- Composition / generic term
- Azithromycin Dihydrate
- Labeler
- TAGI Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190701 / 20261031
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 CARTON in 1 BOX (51224-122-09) / 1 BLISTER PACK in 1 CARTON (51224-122-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 51224-122-09
- 30 TABLET, FILM COATED in 1 BOTTLE (51224-122-30) · 51224-122-30
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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