Home NDC 67296-0710 Acyclovir
Product NDC 67296-0710
11-digit product format 672960710
Labeler code 67296
Product ID 67296-0710_c0a9e9a5-2651-5cca-e053-2995a90a208a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA075382
Marketing category ANDA
Marketing start 2021-01-01
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 2022-12-31
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 67296-0710-1 Acyclovir 20 in 1 BOTTLE TABLET 20 3 67296-0710-2 Acyclovir 30 in 1 BOTTLE TABLET 30 3 67296-0710-7 Acyclovir 15 in 1 BOTTLE TABLET 15 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-0710 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 3 Legacy NDC, 3 package rows 20240712_b93432f0-535c-ab31-e053-2a95a90a03a8.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 67296-0710-1 67296071001 20 TABLET in 1 BOTTLE (67296-0710-1) 20 tablet 2021-10-01 0000-00-00 No No Current 67296-0710-2 67296071002 30 TABLET in 1 BOTTLE (67296-0710-2) 30 tablet 2021-01-01 0000-00-00 No No Current 67296-0710-7 67296071007 15 TABLET in 1 BOTTLE (67296-0710-7) 15 tablet 2021-04-01 0000-00-00 No No Current