Home NDC 85766-115 acyclovir
Product NDC 85766-115
11-digit product format 857660115
Labeler code 85766
Product ID 85766-115_5032177b-fc08-4b34-e063-6294a90a5a17
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form OINTMENT
Route TOPICAL
Labeler Sportpharm LLC
Application ANDA205974
Marketing category ANDA
Marketing start 2020-06-08
Substance ACYCLOVIR
Active strength 50 mg/g
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 50 mg/g
Harmonized Identifiers# Field, Values table Field Values Unii X4HES1O11F Rxcui 197312
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85766-115-15 acyclovir 1 in 1 CARTON OINTMENT 1 2 85766-115-15 acyclovir 15 g in 1 TUBE OINTMENT 15 2
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85766-115-15 85766011515 1 TUBE in 1 CARTON (85766-115-15) / 15 g in 1 TUBE 1 tube 2025-10-31 No No Historical