NDCFind

Ketoconazole 51672-4026-06

Package NDC

51672-4026-06

Product NDC: 51672-4026

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
June 15, 1999
Listing Expires
December 31, 2026
Application
ANDA075319
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Active Ingredients

IngredientStrength
Ketoconazole200 mg/1

Drug Class

Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]

Selected Package

51672-4026-06Selected

30 TABLET in 1 BOTTLE (51672-4026-6)

Other packages for this product(5)

10 BLISTER PACK in 1 BOX (51672-4026-0) / 10 TABLET in 1 BLISTER PACK

100 TABLET in 1 BOTTLE (51672-4026-1)

500 TABLET in 1 BOTTLE (51672-4026-2)

3 BLISTER PACK in 1 BOX (51672-4026-8) / 10 TABLET in 1 BLISTER PACK

5 BLISTER PACK in 1 BOX (51672-4026-9) / 10 TABLET in 1 BLISTER PACK