Home NDC 63739-077 Valacyclovir
Product NDC 63739-077
11-digit product format 637390077
Labeler code 63739
Product ID 63739-077_da6e96b7-28b7-6bed-e053-2995a90a7534
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Valacyclovir
Dosage form TABLET, FILM COATED
Route ORAL
Labeler McKesson Corporation dba SKY Packaging
Application ANDA203047
Marketing category ANDA
Marketing start 2022-03-17
Marketing end 0000-00-00
Substance VALACYCLOVIR HYDROCHLORIDE
Active strength 500 mg/1
Pharmacologic classes DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63739-077 VALACYCLOVIR TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGING] 6 Legacy NDC 20241222_da6ea120-f106-e43e-e053-2995a90a7c83.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 63739-077-10 63739007710 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-077-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK 10 blister pack 2022-03-17 0000-00-00 No No Current