ZOVIRAX - 64455-994-42 - (acyclovir)

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Drug Information of ZOVIRAX

Product NDC: 64455-994
Proprietary Name: ZOVIRAX
Non Proprietary Name: acyclovir
Active Ingredient(s): 50    mg/g & nbsp;   acyclovir
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ZOVIRAX

Product NDC: 64455-994
Labeler Name: BTA PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021478
Marketing Category: NDA
Start Marketing Date: 20041029

Package Information of ZOVIRAX

Package NDC: 64455-994-42
Package Description: 2 g in 1 TUBE (64455-994-42)

NDC Information of ZOVIRAX

NDC Code 64455-994-42
Proprietary Name ZOVIRAX
Package Description 2 g in 1 TUBE (64455-994-42)
Product NDC 64455-994
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name acyclovir
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20041029
Marketing Category Name NDA
Labeler Name BTA PHARMACEUTICALS INC
Substance Name ACYCLOVIR
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Complete Information of ZOVIRAX


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