Home NDC 81288-019 Acyclovir
Product NDC 81288-019
11-digit product format 812880019
Labeler code 81288
Product ID 81288-019_a266fef4-6cf6-4e3e-9df2-a531b7ca7102
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler EMC PHARMA, LLC
Application ANDA210401
Marketing category ANDA
Marketing start 2022-07-29
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 No
Listing certified through 2023-12-31
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 81288-019-01 Acyclovir 100 in 1 BOTTLE TABLET 100 1 81288-019-02 Acyclovir 500 in 1 BOTTLE TABLET 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81288-019 ACYCLOVIR TABLET [EMC PHARMA, LLC] 1 Legacy NDC, 2 package rows 20220729_f74ab549-7636-45c1-bd5f-e79a1492ee2d.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 81288-019-01 81288001901 100 TABLET in 1 BOTTLE (81288-019-01) 100 tablet 2022-07-29 0000-00-00 No No Current 81288-019-02 81288001902 500 TABLET in 1 BOTTLE (81288-019-02) 500 tablet 2022-07-29 0000-00-00 No No Current