Home NDC 67296-1054 Acyclovir
Product NDC 67296-1054
11-digit product format 672961054
Labeler code 67296
Product ID 67296-1054_9c9ed6ec-6ce2-12ed-e053-2995a90a3a3a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA074556
Marketing category ANDA
Marketing start 1997-04-23
Marketing end 0000-00-00
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 2021-12-31
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 67296-1054-2 Acyclovir 20 in 1 BOTTLE TABLET 20 2 67296-1054-3 Acyclovir 30 in 1 BOTTLE TABLET 30 2 67296-1054-5 Acyclovir 15 in 1 BOTTLE TABLET 15 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1054 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 2 Legacy NDC, 3 package rows 20200121_4e403fe2-731d-3453-e054-00144ff88e88.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 67296-1054-2 67296105402 20 TABLET in 1 BOTTLE (67296-1054-2) 20 tablet 1997-04-23 0000-00-00 No No Current 67296-1054-3 67296105403 30 TABLET in 1 BOTTLE (67296-1054-3) 30 tablet 1997-04-23 0000-00-00 No No Current 67296-1054-5 67296105405 15 TABLET in 1 BOTTLE (67296-1054-5) 15 tablet 1997-04-23 0000-00-00 No No Current