Orange Book product · Generic (ANDA)
ACYCLOVIR SODIUM
ACYCLOVIR SODIUM
At a glance
May 13, 1998
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 13, 1998
28 yr 6 mo ago
Today
Pharmaceutical detail
Active ingredient
ACYCLOVIR SODIUM
Strength
EQ 50MG BASE/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 074930
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of ACYCLOVIR SODIUM
- 1989ZOVIRAXBrand (NDA)
NDA 018603 · GLAXOSMITHKLINE
- 2024ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 215404 · FRESENIUS KABI USA
- 2024ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 218111 · SLATE RUN PHARMA
- 2020ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 207919 · DR REDDYS
- 2018ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 206535 · ZYDUS PHARMS
- 2017ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 206606 · ZYDUS PHARMS
- 2017ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 203927 · PHARMOBEDIENT
- 2016ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 205771 · HIKMA
- 2013ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 203701 · EUGIA PHARMA
- 2001ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 075627 · TEVA PARENTERAL
- 1999ACYCLOVIRGeneric (ANDA)
ANDA 075114 · ABBVIE
- 1999ACYCLOVIR SODIUMGeneric (ANDA)
ANDA 075065 · HOSPIRA
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
