acyclovir

Product NDC
63629-1193
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077309
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-1193-150 TABLET in 1 BOTTLE (63629-1193-1) 2021-01-140000-00-00NoCurrent