Home NDC 55154-0199 ACYCLOVIR
Product NDC 55154-0199
11-digit product format 551540199
Labeler code 55154
Product ID 55154-0199_4cc7d67f-35fa-4238-a581-4810645083cf
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Cardinal Health 107, LLC
Application ANDA074889
Marketing category ANDA
Marketing start 2026-05-14
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 55154-0199-0 ACYCLOVIR 10 in 1 BAG CAPSULE 10 1 55154-0199-0 ACYCLOVIR 1 in 1 BLISTER PACK CAPSULE 1 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 55154-0199-0 55154019900 10 BLISTER PACK in 1 BAG (55154-0199-0) / 1 CAPSULE in 1 BLISTER PACK 10 blister pack 2026-05-14 No No Historical