Acyclovir

Product NDC: 50090-1624
11-digit product format: 500901624
Labeler code: 50090
Product ID: 50090-1624_576fa806-8b11-4c7e-815e-49bd39bfbfaf
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: 800 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: 2023-12-31
Current FDA listing: Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50090-1624	ACYCLOVIR TABLET [A-S MEDICATION SOLUTIONS]	28	Legacy NDC	20250501_09b1adb0-945f-4008-b3df-44b467953209.zip

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

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
50090-1624-0	50090162400	35 TABLET in 1 BOTTLE (50090-1624-0)	35 tablet	2015-01-12	0000-00-00	No	No	Current
50090-1624-2	50090162402	70 TABLET in 1 BOTTLE (50090-1624-2)	70 tablet	2015-01-12	0000-00-00	No	No	Current
50090-1624-3	50090162403	40 TABLET in 1 BOTTLE (50090-1624-3)	40 tablet	2018-08-07	0000-00-00	No	No	Current