Home NDC 23155-962 Acyclovir
Product NDC 23155-962
11-digit product format 231550962
Labeler code 23155
Product ID 23155-962_4d5b2bc7-2963-280a-e063-6294a90a06b4
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Avet Pharmaceuticals Inc.
Application ANDA212173
Marketing category ANDA
Marketing start 2026-03-25
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 23155-962-01 Acyclovir 100 in 1 BOTTLE CAPSULE 100 1 23155-962-05 Acyclovir 500 in 1 BOTTLE CAPSULE 500 1
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 23155-962-01 23155096201 100 CAPSULE in 1 BOTTLE (23155-962-01) 100 capsule 2026-03-25 No No Historical 23155-962-05 23155096205 500 CAPSULE in 1 BOTTLE (23155-962-05) 500 capsule 2026-03-25 No No Historical