ACYCLOVIR - acyclovir injection, powder, lyophilized, for solution 
Zydus Lifesciences Limited

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Acyclovir for Injection, USP

PACKAGE LABEL - PRINCIPAL DISPLAY PANEL

Acyclovir for Injection, USP 500 mg/vial - Vial Label

NDC 70771-1081-1

Acyclovir for Injection, USP

Equivalent to

500 mg/vial

acyclovir

For Intravenous Infusion Only

Rx only

zydus pharmaceuticals

Acyclovir sodium Injection, 500 mg/vial

Acyclovir for Injection, USP 500 mg/vial - Carton Label

NDC 70771-1081-6

Acyclovir for Injection, USP

Equivalent to

500 mg/vial

acyclovir

For Intravenous Infusion Only

10 x 500 mg vials

Rx only

zydus pharmaceuticals

Acyclovir for Injection USP, 500 mg/Vial

Acyclovir for Injection, USP 1000 mg/vial - Vial Label

NDC 70771-1082-1

Acyclovir for Injection, USP

Equivalent to

1000 mg/vial

acyclovir

For Intravenous Infusion Only

Rx only

zydus pharmaceuticals

Acyclovir for Injection USP, 1000 mg/vial Vial Label Rx Only Acyclovir sodium Injection, 50 mg/mL

Acyclovir for Injection, USP 1000 mg/vial - Carton Label

NDC 70771-1082-6

Acyclovir for Injection, USP

Equivalent to

1000 mg/vial

acyclovir

For Intravenous Infusion Only

10 x 1000 mg vials

Rx only

zydus pharmaceuticals

Acyclovir for Injection USP, 1000 mg/vial
ACYCLOVIR 
acyclovir injection, powder, lyophilized, for solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1081
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACYCLOVIR SODIUM (UNII: 927L42J563) (ACYCLOVIR - UNII:X4HES1O11F) ACYCLOVIR500 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1081-610 in 1 CARTON; Type 0: Not a Combination Product08/17/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20660608/17/2017
ACYCLOVIR 
acyclovir injection, powder, lyophilized, for solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1082
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACYCLOVIR SODIUM (UNII: 927L42J563) (ACYCLOVIR - UNII:X4HES1O11F) ACYCLOVIR1000 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1082-610 in 1 CARTON; Type 0: Not a Combination Product08/17/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20660608/17/2017
Labeler - Zydus Lifesciences Limited (918596198)
Registrant - Zydus Lifesciences Limited (918596198)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited918596198ANALYSIS(70771-1081, 70771-1082) , MANUFACTURE(70771-1081, 70771-1082)

Revised: 10/2022
Document Id: 6d339b2f-84ca-4174-8774-cbc1b9cec98a
Set id: 3564bff9-794c-4e5d-aead-a1bf3de18ecb
Version: 4
Effective Time: 20221017
 
Zydus Lifesciences Limited