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
- 71205-491_c11b77b5-22be-4867-8752-ffc72a57f768
- Product NDC
- 71205-491
- Form
- TABLET, FILM COATED
- Composition / generic term
- Azithromycin Dihydrate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20261231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-03) · 71205-491-03
- 4 TABLET, FILM COATED in 1 BLISTER PACK (71205-491-04) · 71205-491-04
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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