Acyclovir

Product NDC: 50090-0638
11-digit product format: 500900638
Labeler code: 50090
Product ID: 50090-0638_c810a647-fdb5-4772-97d4-c84e52d0c074
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Acyclovir
Dosage form: TABLET
Route: ORAL
Labeler: A-S Medication Solutions
Application: ANDA075382
Marketing category: ANDA
Marketing start: 2009-10-22
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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50090-0638-0	EA - Each	50090-0638	31ed7665-89ad-475f-b0e0-1ed6b3a457c0	1	2018-09-05
50090-0638-2	EA - Each	50090-0638	38fa5261-f771-4e88-a5f5-a488dbcf2f61	1	2018-09-05
50090-0638-3	EA - Each	50090-0638	56ec9c76-b770-45fa-b146-db938c8d7aa8	1	2022-12-07

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
50090-0638-0	50090063800	35 TABLET in 1 BOTTLE (50090-0638-0)	35 tablet	2014-11-28	0000-00-00	No	No	Current
50090-0638-2	50090063802	70 TABLET in 1 BOTTLE (50090-0638-2)	70 tablet	2014-11-28	0000-00-00	No	No	Current
50090-0638-3	50090063803	40 TABLET in 1 BOTTLE (50090-0638-3)	40 tablet	2022-01-20	0000-00-00	No	No	Current