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
- 0069-3060_1c5f0fcc-88ce-47e9-a128-b7326b7a5a02
- Product NDC
- 0069-3060
- Form
- TABLET, FILM COATED
- Composition / generic term
- azithromycin dihydrate
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 19960718
- Source listing expiry
- 20271231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 BOX (0069-3060-75) / 6 TABLET, FILM COATED in 1 BLISTER PACK · 0069-3060-75
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →