Home NDC 69677-105 Acyclovir
Product NDC 69677-105
11-digit product format 696770105
Labeler code 69677
Product ID 69677-105_686c68c4-53da-6d58-e053-2a91aa0aa746
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler MAS MANAGEMENT GROUP, INC.
Application ANDA204314
Marketing category ANDA
Marketing start 2014-09-10
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 2019-12-31
Current FDA listing Historical FDA.report record 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 69677-105-25 Acyclovir 25 in 1 BOTTLE TABLET 25 1 69677-105-30 Acyclovir 30 in 1 BOTTLE TABLET 30 1 69677-105-35 Acyclovir 35 in 1 BOTTLE TABLET 35 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69677-105 ACYCLOVIR TABLET [MAS MANAGEMENT GROUP, INC.] 1 Legacy NDC, 3 package rows 20180329_686c68c4-53d9-6d58-e053-2a91aa0aa746.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 69677-105-25 69677010525 25 in 1 BOTTLE Historical 69677-105-30 69677010530 30 in 1 BOTTLE Historical 69677-105-35 69677010535 35 in 1 BOTTLE Historical