NDC 51672-4026 – Ketoconazole

Ketoconazole 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51672-4026

Product details

Brand name
Ketoconazole
Generic name
Ketoconazole
Labeler
Sun Pharmaceutical Industries, Inc.
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 (5)

Package NDCDescriptionSince
51672-4026-010 BLISTER PACK in 1 BOX (51672-4026-0) / 10 TABLET in 1 BLISTER PACKJun 15, 1999
51672-4026-1100 TABLET in 1 BOTTLE (51672-4026-1)Jun 15, 1999
51672-4026-2500 TABLET in 1 BOTTLE (51672-4026-2)Jun 15, 1999
51672-4026-83 BLISTER PACK in 1 BOX (51672-4026-8) / 10 TABLET in 1 BLISTER PACKJun 15, 1999
51672-4026-95 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACKJun 15, 1999

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