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NDC 71335-1652-01 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 Bryant Ranch Prepack. 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: 71335-1652-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Ketoconazole

Product Information

NDC	71335-1652
Product ID	71335-1652_ad97ec3a-f51c-484b-87ec-8b3fb7a55089
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
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	Bryant Ranch Prepack
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	ANDA210457
Listing Certified Through	2022-12-31

Package

NDC 71335-1652-01 (71335165201)

Pricing Information	N/A
NDC Package Code	71335-1652-1
Billing NDC	71335165201
Package	10 TABLET in 1 BOTTLE (71335-1652-1)
Marketing Start Date	2020-06-26
NDC Exclude Flag	N