Home NDC 68071-5094 acyclovir
Product NDC 68071-5094
11-digit product format 680715094
Labeler code 68071
Product ID 68071-5094_bbf28d05-803d-7c6d-e053-2a95a90aa942
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler NuCare Pharmaceuticals,Inc.
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 68071-5094-1 acyclovir 100 in 1 BOTTLE TABLET 100 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68071-5094 ACYCLOVIR TABLET [NUCARE PHARMACEUTICALS,INC.] 2 Legacy NDC, 1 package rows 20210223_95b0c656-f87c-8ba9-e053-2a95a90ae06c.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 68071-5094-1 68071509401 100 TABLET in 1 BOTTLE (68071-5094-1) 100 tablet 2019-10-25 0000-00-00 No No Current