Home NDC 33261-419 Acyclovir
Product NDC 33261-419
11-digit product format 332610419
Labeler code 33261
Product ID 33261-419_7a30fb41-2a84-4afb-a155-46dba2cfb76a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Aidarex Pharmaceuticals LLC
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 2019-12-31
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 33261-419-30 Acyclovir 30 in 1 BOTTLE CAPSULE 30 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 33261-419 ACYCLOVIR CAPSULE ACYCLOVIR TABLET [AIDAREX PHARMACEUTICALS LLC] 3 Legacy NDC, 1 package rows 20120913_68227df2-cac6-4799-8dcd-8c2f42204315.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 33261-419-30 33261041930 30 in 1 BOTTLE Historical