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
- 68180-862_ca28af23-6ff4-43a9-9f5f-3a2af0a9c005
- Product NDC
- 68180-862
- Form
- TABLET, FILM COATED
- Composition / generic term
- azithromycin
- Labeler
- Lupin Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150818
- Source listing expiry
- 20271231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 CONTAINER (68180-862-06) · 68180-862-06
- 1 BLISTER PACK in 1 CARTON (68180-862-11) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 68180-862-11
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 →