Acyclovir - 0093-8940-19 - (Acyclovir)

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Drug Information of Acyclovir

Product NDC: 0093-8940
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 200    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 0093-8940
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074578
Marketing Category: ANDA
Start Marketing Date: 19970423

Package Information of Acyclovir

Package NDC: 0093-8940-19
Package Description: 1 CAPSULE in 1 BLISTER PACK (0093-8940-19)

NDC Information of Acyclovir

NDC Code 0093-8940-19
Proprietary Name Acyclovir
Package Description 1 CAPSULE in 1 BLISTER PACK (0093-8940-19)
Product NDC 0093-8940
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19970423
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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