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
- 68094-799_30012db7-75f6-47ef-838b-301c9a3b2c8e
- Product NDC
- 68094-799
- Form
- TABLET, FILM COATED
- Composition / generic term
- Azithromycin dihydrate
- Labeler
- Precision Dose, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240215
- Source listing expiry
- 20271231
Source-listed ingredients
- AZITHROMYCIN DIHYDRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (68094-799-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 68094-799-03
- 3 CARTON in 1 BOX (68094-799-09) / 1 BLISTER PACK in 1 CARTON / 3 TABLET, FILM COATED in 1 BLISTER PACK · 68094-799-09
- 30 TABLET, FILM COATED in 1 BOTTLE (68094-799-30) · 68094-799-30
- 100 TABLET, FILM COATED in 1 BOTTLE (68094-799-50) · 68094-799-50
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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