Home NDC 67296-0240 Acyclovir
Product NDC 67296-0240
11-digit product format 672960240
Labeler code 67296
Product ID 67296-0240_9c9a724e-9779-34d5-e053-2a95a90a50c4
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA074578
Marketing category ANDA
Marketing start 1997-04-23
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 67296-0240-1 Acyclovir 35 in 1 BOTTLE CAPSULE 35 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-0240 ACYCLOVIR CAPSULE [REDPHARM DRUG, INC.] 3 Legacy NDC, 1 package rows 20200121_4199a62e-b61e-31a2-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 67296-0240-1 67296024001 35 CAPSULE in 1 BOTTLE (67296-0240-1) 35 capsule 1997-04-23 0000-00-00 No No Current