Home NDC 51655-965 acyclovir
Product NDC 51655-965
11-digit product format 516550965
Labeler code 51655
Product ID 51655-965_4a928f78-59d0-cddc-e063-6394a90aac53
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Northwind Health Company, LLC
Application ANDA204313
Marketing category ANDA
Marketing start 2023-06-27
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 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base acyclovir
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACYCLOVIR 200 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii X4HES1O11F Rxcui 197310
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51655-965-52 acyclovir 30 in 1 BOTTLE, PLASTIC CAPSULE 30 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51655-965 ACYCLOVIR CAPSULE [NORTHWIND PHARMACEUTICALS, LLC] 2 Current NDC, 1 package rows 20240814_ff9776b3-a248-e1ea-e053-6294a90aeb7b.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51655-965-52 51655096552 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-965-52) 30 capsule 2023-06-27 No No Historical