Home NDC 0440-7033 acyclovir
Product NDC 0440-7033
11-digit product format 004407033
Labeler code 0440
Product ID 0440-7033_cdbd882b-80ec-4d72-85b2-835650f08146
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler Liberty Pharmaceuticals, Inc.
Application ANDA077309
Marketing category ANDA
Marketing start 2006-03-13
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 800 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 E
Listing certified through 2018-12-31
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 0440-7033-81 acyclovir 300 in 1 BOTTLE TABLET 300 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0440-7033 ACYCLOVIR TABLET [LIBERTY PHARMACEUTICALS, INC.] 1 Legacy NDC, 1 package rows 20160813_495bb417-880e-4af0-9374-c2ef7ae82c7b.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 0440-7033-81 00440703381 300 in 1 BOTTLE Historical