Acyclovir

Product NDC
67296-1219
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
RedPharm Drug, Inc.
Application
ANDA074556
Marketing category
ANDA
Substance
ACYCLOVIR
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
67296-1219-550 TABLET in 1 BOTTLE (67296-1219-5) 1997-04-300000-00-00NoCurrent
67296-1219-66 TABLET in 1 BOTTLE (67296-1219-6) 1997-04-300000-00-00NoCurrent
67296-1219-835 TABLET in 1 BOTTLE (67296-1219-8) 1997-04-300000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
4f2d72eb-339e-12b1-e054-00144ff88e88RedPharm Drug, Inc.2020-01-20HUMAN PRESCRIPTION DRUG LABEL2