Acyclovir - 0093-8943-19 - (Acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 0093-8943
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 400    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 0093-8943
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074556
Marketing Category: ANDA
Start Marketing Date: 19970423

Package Information of Acyclovir

Package NDC: 0093-8943-19
Package Description: 1 TABLET in 1 BLISTER PACK (0093-8943-19)

NDC Information of Acyclovir

NDC Code 0093-8943-19
Proprietary Name Acyclovir
Package Description 1 TABLET in 1 BLISTER PACK (0093-8943-19)
Product NDC 0093-8943
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970423
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name ACYCLOVIR
Strength Number 400
Strength Unit mg/1
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 Acyclovir


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