Home NDC 67296-1219 Acyclovir
Product NDC 67296-1219
11-digit product format 672961219
Labeler code 67296
Product ID 67296-1219_9c9f1f5c-8649-15d3-e053-2995a90afc6e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA074556
Marketing category ANDA
Marketing start 1997-04-30
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 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 67296-1219-5 Acyclovir 50 in 1 BOTTLE TABLET 50 2 67296-1219-6 Acyclovir 6 in 1 BOTTLE TABLET 6 2 67296-1219-8 Acyclovir 35 in 1 BOTTLE TABLET 35 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1219 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 2 Legacy NDC, 3 package rows 20200121_4f2d72eb-339e-12b1-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 67296-1219-5 67296121905 50 TABLET in 1 BOTTLE (67296-1219-5) 50 tablet 1997-04-30 0000-00-00 No No Current 67296-1219-6 67296121906 6 TABLET in 1 BOTTLE (67296-1219-6) 6 tablet 1997-04-30 0000-00-00 No No Current 67296-1219-8 67296121908 35 TABLET in 1 BOTTLE (67296-1219-8) 35 tablet 1997-04-30 0000-00-00 No No Current