Acyclovir

Product NDC
50090-6844
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203834
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6844-090 TABLET in 1 BOTTLE (50090-6844-0) 2023-11-29NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Acyclovir Tablets, USP Rx onlyA-S Medication Solutions2023-12-05HUMAN PRESCRIPTION DRUG LABEL1