Nizoral - 50580-895-15 - (Ketoconazole)

Alphabetical Index


Drug Information of Nizoral

Product NDC: 50580-895
Proprietary Name: Nizoral
Non Proprietary Name: Ketoconazole
Active Ingredient(s): 10    mg/mL & nbsp;   Ketoconazole
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Nizoral

Product NDC: 50580-895
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020310
Marketing Category: NDA
Start Marketing Date: 19990401

Package Information of Nizoral

Package NDC: 50580-895-15
Package Description: 10 PACKET in 1 CARTON (50580-895-15) > 6 mL in 1 PACKET

NDC Information of Nizoral

NDC Code 50580-895-15
Proprietary Name Nizoral
Package Description 10 PACKET in 1 CARTON (50580-895-15) > 6 mL in 1 PACKET
Product NDC 50580-895
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ketoconazole
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 19990401
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name KETOCONAZOLE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Nizoral


General Information