Home NDC 71335-1757 ACYCLOVIR
Product NDC 71335-1757
11-digit product format 713351757
Labeler code 71335
Product ID 71335-1757_45462e20-c9a7-48c1-a1b4-13a1be79a3e5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ACYCLOVIR
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA074891
Marketing category ANDA
Marketing start 2013-08-08
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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ACYCLOVIR
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACYCLOVIR 400 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii X4HES1O11F Rxcui 197311
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71335-1757-1 ACYCLOVIR 35 in 1 BOTTLE TABLET 35 102 71335-1757-2 ACYCLOVIR 90 in 1 BOTTLE TABLET 90 102
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71335-1757 ACYCLOVIR TABLET [BRYANT RANCH PREPACK] 102 Current NDC, Legacy NDC, 2 package rows 20240518_c0e41bf9-e141-404e-9952-aeeb705958b4.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71335-1757-1 71335175701 35 TABLET in 1 BOTTLE (71335-1757-1) 35 tablet 2022-01-28 0000-00-00 No No Current 71335-1757-2 71335175702 90 TABLET in 1 BOTTLE (71335-1757-2) 90 tablet 2021-01-04 0000-00-00 No No Current