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NDC 51672-4026-00 Ketoconazole 200 mg/1 Details

Ketoconazole 200 mg/1

Ketoconazole is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is KETOCONAZOLE.

MedlinePlus Drug Summary

Ketoconazole is used to treat fungal infections when other medications are not available or cannot be tolerated. Ketoconazole should not be used to treat fungal meningitis (infection of the membranes surrounding the brain and spinal cord caused by a fungus) or fungal nail infections. Ketoconazole is in a class of antifungals called imidazoles. It works by slowing the growth of fungi that cause infection.

Related Packages: 51672-4026-00
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ketoconazole

Product Information

NDC	51672-4026
Product ID	51672-4026_da3f4801-92d7-4031-b690-e6d559c383cb
Associated GPIs	11404040000310
GCN Sequence Number	009544
GCN Sequence Number Description	ketoconazole TABLET 200 MG ORAL
HIC3	W3B
HIC3 Description	ANTIFUNGAL AGENTS
GCN	42590
HICL Sequence Number	004132
HICL Sequence Number Description	KETOCONAZOLE
Brand/Generic	Generic
Proprietary Name	Ketoconazole
Proprietary Name Suffix	n/a
Non-Proprietary Name	Ketoconazole
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	200
Active Ingredient Units	mg/1
Substance Name	KETOCONAZOLE
Labeler Name	Taro Pharmaceuticals U.S.A., Inc.
Pharmaceutical Class	Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA075319
Listing Certified Through	2024-12-31

Package

NDC 51672-4026-00 (51672402600)

Pricing Information	N/A
NDC Package Code	51672-4026-0
Billing NDC	51672402600
Package	10 BLISTER PACK in 1 BOX (51672-4026-0) / 10 TABLET in 1 BLISTER PACK
Marketing Start Date	1999-06-15
NDC Exclude Flag	N