Home NDC 70518-4186 ACYCLOVIR
Product NDC 70518-4186
11-digit product format 705184186
Labeler code 70518
Product ID 70518-4186_3ff281aa-ddd3-a441-e063-6394a90a6946
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ACYCLOVIR
Dosage form TABLET
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA074891
Marketing category ANDA
Marketing start 2024-09-25
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 Additional Listing Data#
Finished product Yes
Brand name base ACYCLOVIR
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACYCLOVIR 800 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii X4HES1O11F Rxcui 197313
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-4186-0 ACYCLOVIR 10 in 1 BOTTLE, PLASTIC TABLET 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-4186 ACYCLOVIR TABLET [REMEDYREPACK INC.] 1 Current NDC, 1 package rows 20240927_c1744e01-0e40-4851-8ffc-c3bf29dd7c2b.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70518-4186-0 70518418600 10 TABLET in 1 BOTTLE, PLASTIC (70518-4186-0) 10 tablet 2024-09-25 No No Current