NDC 71335-0439 – Ketoconazole

Ketoconazole 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0439

Product details

Brand name
Ketoconazole
Generic name
Ketoconazole
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075319
Marketed since
June 15, 1999
Listing expires
December 31, 2026
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Ketoconazole →

Package NDC codes (8)

Package NDCDescriptionSince
71335-0439-110 TABLET in 1 BOTTLE (71335-0439-1)Apr 28, 2010
71335-0439-230 TABLET in 1 BOTTLE (71335-0439-2)Apr 28, 2010
71335-0439-340 TABLET in 1 BOTTLE (71335-0439-3)Apr 28, 2010
71335-0439-460 TABLET in 1 BOTTLE (71335-0439-4)Apr 28, 2010
71335-0439-58 TABLET in 1 BOTTLE (71335-0439-5)Apr 28, 2010
71335-0439-67 TABLET in 1 BOTTLE (71335-0439-6)Apr 28, 2010
71335-0439-714 TABLET in 1 BOTTLE (71335-0439-7)Apr 28, 2010
71335-0439-890 TABLET in 1 BOTTLE (71335-0439-8)Apr 28, 2010

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