Acyclovir

Product NDC: 63739-682
11-digit product format: 637390682
Labeler code: 63739
Product ID: 63739-682_b3c45f2f-e5db-af99-e053-2a95a90a4ad9
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: McKesson Corporation dba SKY Packaging
Application: ANDA075382
Marketing category: ANDA
Marketing start: 2009-10-22
Marketing end: 2020-12-31
Substance: ACYCLOVIR
Active strength: 400 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: 0000-00-00
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63739-682-10	2020-07-22	C162847	48780-1	ab0e2407-2f1b-f274-e053-dbdaa90a6471	06c03569-ba13-436d-97bc-df7285652330

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
63739-682-10	EA - Each	63739-682	506e69c9-a6d4-49d2-8edb-5a46d09f3f99	1	2015-04-03