Home NDC 67296-1034 acyclovir
Product NDC 67296-1034
11-digit product format 672961034
Labeler code 67296
Product ID 67296-1034_d60f9a37-90c2-7879-e053-2995a90a4d55
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA077309
Marketing category ANDA
Marketing start 2006-03-13
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 2023-12-31
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 67296-1034-3 acyclovir 35 in 1 BOTTLE TABLET 35 3 67296-1034-5 acyclovir 50 in 1 BOTTLE TABLET 50 3 67296-1034-6 acyclovir 6 in 1 BOTTLE TABLET 6 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1034 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 3 Legacy NDC, 3 package rows 20220121_4e2d06ed-7b2f-26d5-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 67296-1034-3 67296103403 35 TABLET in 1 BOTTLE (67296-1034-3) 35 tablet 2006-03-13 0000-00-00 No No Current 67296-1034-5 67296103405 50 TABLET in 1 BOTTLE (67296-1034-5) 50 tablet 2006-03-13 0000-00-00 No No Current 67296-1034-6 67296103406 6 TABLET in 1 BOTTLE (67296-1034-6) 6 tablet 2006-03-13 0000-00-00 No No Current