NDC 71335-2235 – Fluconazole

Fluconazole 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2235

Product details

Brand name
Fluconazole
Generic name
Fluconazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077731
Marketed since
October 7, 2008
Listing expires
December 31, 2026
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Fluconazole →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2235-04 TABLET in 1 BOTTLE (71335-2235-0)Sep 18, 2023
71335-2235-130 TABLET in 1 BOTTLE (71335-2235-1)May 6, 2024
71335-2235-212 TABLET in 1 BOTTLE (71335-2235-2)Sep 6, 2024
71335-2235-3100 TABLET in 1 BOTTLE (71335-2235-3)Sep 6, 2024
71335-2235-43 TABLET in 1 BOTTLE (71335-2235-4)Sep 6, 2024
71335-2235-528 TABLET in 1 BOTTLE (71335-2235-5)Sep 6, 2024
71335-2235-61 TABLET in 1 BOTTLE (71335-2235-6)Sep 6, 2024
71335-2235-72 TABLET in 1 BOTTLE (71335-2235-7)Oct 16, 2023
71335-2235-814 TABLET in 1 BOTTLE (71335-2235-8)Oct 11, 2023
71335-2235-98 TABLET in 1 BOTTLE (71335-2235-9)Sep 6, 2024

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