Home NDC 67296-0656 Acyclovir
Product NDC 67296-0656
11-digit product format 672960656
Labeler code 67296
Product ID 67296-0656_9c9ae05a-bc99-79b6-e053-2a95a90a88ca
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA075090
Marketing category ANDA
Marketing start 2009-10-22
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 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 67296-0656-1 Acyclovir 35 in 1 BOTTLE CAPSULE 35 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-0656 ACYCLOVIR CAPSULE [REDPHARM DRUG, INC.] 4 Legacy NDC, 1 package rows 20200121_415a816c-ede9-390d-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 67296-0656-1 67296065601 35 CAPSULE in 1 BOTTLE (67296-0656-1) 35 capsule 2009-10-22 0000-00-00 No No Current