United States · FDA National Drug Code directory
Zithromax
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
- 0069-3140_1c5f0fcc-88ce-47e9-a128-b7326b7a5a02
- Product NDC
- 0069-3140
- Form
- POWDER, FOR SUSPENSION
- Composition / generic term
- azithromycin dihydrate
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 19951019
- Source listing expiry
- 20271231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 200 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0069-3140-19) / 30 mL in 1 BOTTLE · 0069-3140-19
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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