Home NDC 71209-006
Acyclovir
Product NDC 71209-006
11-digit product format 712090006
Labeler code 71209
Product ID 71209-006_4c64f761-cab6-4360-9561-89b32c3ec030
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Cadila Pharmaceuticals Limited
Application ANDA202168
Marketing category ANDA
Marketing start 2017-03-23
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 197311, 197313
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71209-006-05 Acyclovir 100 in 1 BOTTLE TABLET 100 6 71209-006-10 Acyclovir 500 in 1 BOTTLE TABLET 500 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71209-006 ACYCLOVIR TABLET [CADILA PHARMACEUTICALS LIMITED] 5 Current NDC, Legacy NDC, 2 package rows 20221231_acef88f4-6456-4092-993f-27e1496097c7.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 71209-006-05 71209000605 100 TABLET in 1 BOTTLE (71209-006-05) 100 tablet 2018-11-20 0000-00-00 No No Current 71209-006-10 71209000610 500 TABLET in 1 BOTTLE (71209-006-10) 500 tablet 2018-11-20 0000-00-00 No No Current