Home NDC 0093-3630 Acyclovir
Product NDC 0093-3630
11-digit product format 000933630
Labeler code 0093
Product ID 0093-3630_41d48b5c-d1d0-66d0-e063-6294a90ab384
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form CREAM
Route TOPICAL
Labeler Teva Pharmaceuticals USA, Inc.
Application NDA021478
Marketing category NDA AUTHORIZED GENERIC
Marketing start 2019-08-29
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 141859
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0093-3630-20 Acyclovir 5 g in 1 TUBE CREAM 5 7 0093-3630-20 Acyclovir 1 in 1 CARTON CREAM 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0093-3630 ACYCLOVIR CREAM [TEVA PHARMACEUTICALS USA, INC.] 6 Current NDC, Legacy NDC, 2 package rows 20231116_103f29b8-2c13-4917-a446-59d3246d48d1.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0093-3630-20 00093363020 1 TUBE in 1 CARTON (0093-3630-20) / 5 g in 1 TUBE 1 tube 2019-08-29 0000-00-00 No No Current