Acyclovir

Product NDC: 50090-1568
11-digit product format: 500901568
Labeler code: 50090
Product ID: 50090-1568_3b1281ac-3206-4a60-bcc2-937c3936e8a0
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA203834
Marketing category: ANDA
Marketing start: 2013-11-29
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: 2022-12-31
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
50090-1568-0	50090156800	90 TABLET in 1 BOTTLE (50090-1568-0)	90 tablet	2014-12-22	0000-00-00	No	No	Current
50090-1568-1	50090156801	21 TABLET in 1 BOTTLE (50090-1568-1)	21 tablet	2016-04-18	0000-00-00	No	No	Current