Home NDC 67296-1185 acyclovir
Product NDC 67296-1185
11-digit product format 672961185
Labeler code 67296
Product ID 67296-1185_d60ff571-d1ca-0675-e053-2995a90a15aa
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form TABLET
Route ORAL
Labeler RedPharm Drug, Inc.
Application ANDA204314
Marketing category ANDA
Marketing start 2014-09-10
Marketing end 0000-00-00
Substance ACYCLOVIR
Active strength 400 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 2023-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67296-1185-2 acyclovir 20 in 1 BOTTLE TABLET 20 3 67296-1185-3 acyclovir 30 in 1 BOTTLE TABLET 30 3 67296-1185-5 acyclovir 15 in 1 BOTTLE TABLET 15 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1185 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 3 Legacy NDC, 2 package rows 20220121_5c50afc5-12fb-86f5-e053-2a91aa0a350b.zip 67296-1185 ACYCLOVIR TABLET [REDPHARM DRUG, INC.] 1 Legacy NDC, 1 package rows 20180516_6c5662a1-df2e-a627-e053-2a91aa0a7844.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 67296-1185-2 67296118502 20 TABLET in 1 BOTTLE (67296-1185-2) 20 tablet 2014-09-10 0000-00-00 No No Current 67296-1185-3 67296118503 30 TABLET in 1 BOTTLE (67296-1185-3) 30 tablet 2014-09-10 0000-00-00 No No Current 67296-1185-5 67296118505 15 in 1 BOTTLE Historical