Acyclovir

Product NDC
71335-2555
11-digit product format
713352555
Labeler code
71335
Product ID
71335-2555_904c860d-4d2e-4360-ab30-4242e43d379e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Acyclovir
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA209366
Marketing category
ANDA
Marketing start
2020-08-15
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
X4HES1O11FACYCLOVIR59277-89-3ACYCLOVIR

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2555-071335255500500 TABLET in 1 BOTTLE (71335-2555-0) 500 tablet2025-01-23NoNoHistorical
71335-2555-17133525550125 TABLET in 1 BOTTLE (71335-2555-1) 25 tablet2025-01-23NoNoHistorical
71335-2555-27133525550235 TABLET in 1 BOTTLE (71335-2555-2) 35 tablet2025-01-23NoNoHistorical
71335-2555-37133525550330 TABLET in 1 BOTTLE (71335-2555-3) 30 tablet2025-01-23NoNoHistorical
71335-2555-47133525550460 TABLET in 1 BOTTLE (71335-2555-4) 60 tablet2025-01-23NoNoHistorical
71335-2555-57133525550550 TABLET in 1 BOTTLE (71335-2555-5) 50 tablet2025-01-23NoNoHistorical
71335-2555-67133525550610 TABLET in 1 BOTTLE (71335-2555-6) 10 tablet2025-01-23NoNoHistorical
71335-2555-77133525550740 TABLET in 1 BOTTLE (71335-2555-7) 40 tablet2025-01-23NoNoHistorical
71335-2555-87133525550821 TABLET in 1 BOTTLE (71335-2555-8) 21 tablet2025-01-23NoNoHistorical
71335-2555-97133525550990 TABLET in 1 BOTTLE (71335-2555-9) 90 tablet2025-01-23NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Acyclovir Tablets, USPBryant Ranch Prepack2025-01-23HUMAN PRESCRIPTION DRUG LABEL1