VALGANCICLOVIR HYDROCHLORIDE

Product NDC: 63739-357
11-digit product format: 637390357
Labeler code: 63739
Product ID: 63739-357_b4cb3179-ae53-8238-e053-2a95a90ab6e0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: VALGANCICLOVIR HYDROCHLORIDE
Dosage form: TABLET
Route: ORAL
Labeler: Mckesson Corporation DBA SKY Packaginng
Application: ANDA204750
Marketing category: ANDA
Marketing start: 2016-03-31
Marketing end: 0000-00-00
Substance: VALGANCICLOVIR HYDROCHLORIDE
Active strength: 450 mg/1
Pharmacologic classes: Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [EXT],Nucleoside Analog Antiviral [EPC]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-357-33	2020-07-22	C162847	48780-1	ab0e2407-2b2d-f274-e053-dbdaa90a6471	e937f02d-a76c-4a2f-b9ad-84897391580f

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-357-33	EA - Each	63739-357	e46a3c93-d8ee-4721-a6a9-c4a324c4d24c	1	2017-06-15

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4P3T9QF9NZ	VALGANCICLOVIR HYDROCHLORIDE	175865-59-5	VALGANCICLOVIR HYDROCHLORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63739-357-33	63739035733	3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-357-33) > 10 TABLET in 1 BLISTER PACK	3 blister pack	2017-05-31	0000-00-00	No	No	Current