Home NDC 68071-3909
acyclovir
Product NDC 68071-3909
11-digit product format 680713909
Labeler code 68071
Product ID 68071-3909_41d5ae23-2733-325f-e063-6294a90ab07c
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form OINTMENT
Route TOPICAL
Labeler NuCare Pharmaceuticals, Inc.
Application ANDA205510
Marketing category ANDA
Marketing start 2017-07-31
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 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base acyclovir
Listing expiration 2026-12-31
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 68071-3909-5 acyclovir 1 in 1 CARTON OINTMENT 1 3 68071-3909-5 acyclovir 15 g in 1 TUBE OINTMENT 15 3
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 68071-3909-5 68071390905 1 TUBE in 1 CARTON (68071-3909-5) / 15 g in 1 TUBE 1 tube 2025-10-23 No No Current