United States · FDA National Drug Code directory
Fluconazole
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
- 71335-1895_0a2b1160-1a6c-414e-91b5-f3d2e3657c1f
- Product NDC
- 71335-1895
- Form
- TABLET
- Composition / generic term
- Fluconazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210422
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUCONAZOLE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET in 1 BOTTLE (71335-1895-0) · 71335-1895-0
- 30 TABLET in 1 BOTTLE (71335-1895-1) · 71335-1895-1
- 12 TABLET in 1 BOTTLE (71335-1895-2) · 71335-1895-2
- 100 TABLET in 1 BOTTLE (71335-1895-3) · 71335-1895-3
- 3 TABLET in 1 BOTTLE (71335-1895-4) · 71335-1895-4
- 28 TABLET in 1 BOTTLE (71335-1895-5) · 71335-1895-5
- 1 TABLET in 1 BOTTLE (71335-1895-6) · 71335-1895-6
- 2 TABLET in 1 BOTTLE (71335-1895-7) · 71335-1895-7
- 14 TABLET in 1 BOTTLE (71335-1895-8) · 71335-1895-8
- 8 TABLET in 1 BOTTLE (71335-1895-9) · 71335-1895-9
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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