NDC 63739-076

Valganciclovir

Valganciclovir

Valganciclovir is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Mckesson Corporation Dba Sky Packaging. The primary component is Valganciclovir Hydrochloride.

Product ID63739-076_d96b7eea-05f5-0b8e-e053-2995a90a4db4
NDC63739-076
Product TypeHuman Prescription Drug
Proprietary NameValganciclovir
Generic NameValganciclovir
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-03-07
Marketing CategoryANDA /
Application NumberANDA205166
Labeler NameMcKesson Corporation DBA SKY Packaging
Substance NameVALGANCICLOVIR HYDROCHLORIDE
Active Ingredient Strength450 mg/1
Pharm ClassesCytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], DNA Polymerase Inhibitors [MoA], Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63739-076-33

3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-076-33) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2022-03-07
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Valganciclovir" or generic name "Valganciclovir"

NDCBrand NameGeneric Name
0603-6330ValganciclovirValganciclovir hydrochloride
0904-6796ValganciclovirValganciclovir
16714-765ValganciclovirValganciclovir
27241-158ValganciclovirValganciclovir
31722-832ValganciclovirValganciclovir
31722-837VALGANCICLOVIRVALGANCICLOVIR HYDROCHLORIDE
42291-875ValganciclovirValganciclovir hydrochloride
48433-124ValganciclovirValganciclovir
50268-787ValganciclovirValganciclovir
55111-762ValganciclovirValganciclovir
59651-444ValganciclovirValganciclovir hydrochloride powder,
60429-846ValganciclovirValganciclovir
63629-2288ValganciclovirValganciclovir hydrochloride
63739-076ValganciclovirValganciclovir
64380-153ValganciclovirValganciclovir hydrochloride
68084-965ValganciclovirValganciclovir
69097-277ValganciclovirValganciclovir
0004-0038Valcytevalganciclovir

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