Home NDC 67296-1108 ACYCLOVIR
Product NDC 67296-1108
11-digit product format 672961108
Labeler code 67296
Product ID 67296-1108_d60fdf62-9205-4fa8-e053-2995a90adb18
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name ACYCLOVIR
Dosage form CAPSULE
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA075677
Marketing category ANDA
Marketing start 2006-03-20
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 200 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 67296-1108-8 ACYCLOVIR 35 in 1 BOTTLE CAPSULE 35 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1108 ACYCLOVIR CAPSULE [REDPHARM DRUG, INC.] 5 Legacy NDC, 1 package rows 20220121_4e8f535c-057d-0ddf-e054-00144ff8d46c.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 67296-1108-8 67296110808 35 CAPSULE in 1 BOTTLE (67296-1108-8) 35 capsule 2006-03-20 0000-00-00 No No Current