acyclovir

Product NDC: 63629-7613
11-digit product format: 636297613
Labeler code: 63629
Product ID: 63629-7613_6c990a79-2585-41ce-b48e-c2e748976f9a
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA204314
Marketing category: ANDA
Marketing start: 2014-09-10
Marketing end: 0000-00-00
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: 2020-12-31
Current FDA listing: Historical FDA.report record

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
X4HES1O11F	ACYCLOVIR	59277-89-3	ACYCLOVIR

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-7613-1	63629761301	35 TABLET in 1 BOTTLE (63629-7613-1)	35 tablet	2016-02-10	0000-00-00	No	No	Current
63629-7613-2	63629761302	90 TABLET in 1 BOTTLE (63629-7613-2)	90 tablet	2018-05-21	0000-00-00	No	No	Current