NOXAFIL - 0085-1328-01 - (posaconazole)

Alphabetical Index


Drug Information of NOXAFIL

Product NDC: 0085-1328
Proprietary Name: NOXAFIL
Non Proprietary Name: posaconazole
Active Ingredient(s): 40    mg/mL & nbsp;   posaconazole
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of NOXAFIL

Product NDC: 0085-1328
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022003
Marketing Category: NDA
Start Marketing Date: 20060915

Package Information of NOXAFIL

Package NDC: 0085-1328-01
Package Description: 1 BOTTLE, GLASS in 1 CARTON (0085-1328-01) > 105 mL in 1 BOTTLE, GLASS

NDC Information of NOXAFIL

NDC Code 0085-1328-01
Proprietary Name NOXAFIL
Package Description 1 BOTTLE, GLASS in 1 CARTON (0085-1328-01) > 105 mL in 1 BOTTLE, GLASS
Product NDC 0085-1328
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name posaconazole
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20060915
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name POSACONAZOLE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of NOXAFIL


General Information