Acyclovir - 55154-8295-0 - (Acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 55154-8295
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 200    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 55154-8295
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074556
Marketing Category: ANDA
Start Marketing Date: 19970423

Package Information of Acyclovir

Package NDC: 55154-8295-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-8295-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Acyclovir

NDC Code 55154-8295-0
Proprietary Name Acyclovir
Package Description 10 BLISTER PACK in 1 BAG (55154-8295-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-8295
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 Cardinal Health
Substance Name ACYCLOVIR
Strength Number 200
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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