Home NDC 50090-0643
acyclovir
Product NDC 50090-0643
11-digit product format 500900643
Labeler code 50090
Product ID 50090-0643_fd470293-c61f-4e25-b8a9-ebe00201cfde
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler A-S Medication Solutions
Application ANDA077309
Marketing category ANDA
Marketing start 2007-06-09
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 400 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 2022-12-31
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 50090-0643-0 acyclovir 90 in 1 BOTTLE TABLET 90 2 50090-0643-1 acyclovir 21 in 1 BOTTLE TABLET 21 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50090-0643 ACYCLOVIR TABLET [A-S MEDICATION SOLUTIONS] 2 Legacy NDC, 2 package rows 20210318_d846dc43-d7d0-435a-8b61-c51b39c664aa.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 50090-0643-0 50090064300 90 TABLET in 1 BOTTLE (50090-0643-0) 90 tablet 2014-11-28 0000-00-00 No No Current 50090-0643-1 50090064301 21 TABLET in 1 BOTTLE (50090-0643-1) 21 tablet 2019-10-23 0000-00-00 No No Current