Valacyclovir Hydrochloride

Product NDC
71335-1485
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
valacyclovir
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078518
Marketing category
ANDA
Substance
VALACYCLOVIR HYDROCHLORIDE
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71335-1485-060 TABLET, FILM COATED in 1 BOTTLE (71335-1485-0) 2020-01-230000-00-00NoCurrent
71335-1485-130 TABLET, FILM COATED in 1 BOTTLE (71335-1485-1) 2020-01-230000-00-00NoCurrent
71335-1485-221 TABLET, FILM COATED in 1 BOTTLE (71335-1485-2) 2020-01-230000-00-00NoCurrent
71335-1485-320 TABLET, FILM COATED in 1 BOTTLE (71335-1485-3) 2020-01-230000-00-00NoCurrent
71335-1485-44 TABLET, FILM COATED in 1 BOTTLE (71335-1485-4) 2020-01-230000-00-00NoCurrent
71335-1485-510 TABLET, FILM COATED in 1 BOTTLE (71335-1485-5) 2020-01-230000-00-00NoCurrent
71335-1485-66 TABLET, FILM COATED in 1 BOTTLE (71335-1485-6) 2020-01-230000-00-00NoCurrent
71335-1485-715 TABLET, FILM COATED in 1 BOTTLE (71335-1485-7) 2020-01-230000-00-00NoCurrent
71335-1485-88 TABLET, FILM COATED in 1 BOTTLE (71335-1485-8) 2020-01-230000-00-00NoCurrent
71335-1485-990 TABLET, FILM COATED in 1 BOTTLE (71335-1485-9) 2020-01-230000-00-00NoCurrent