Home NDC 67046-335 Acyclovir
Product NDC 67046-335
11-digit product format 670460335
Labeler code 67046
Product ID 67046-335_a8524172-91fc-6eb2-e053-2a95a90a1cae
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Contract Pharmacy Services-PA
Application ANDA203834
Marketing category ANDA
Marketing start 2020-06-15
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 2021-12-31
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 67046-335-30 Acyclovir 30 in 1 BLISTER PACK TABLET 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67046-335 ACYCLOVIR TABLET [CONTRACT PHARMACY SERVICES-PA] 1 Legacy NDC, 1 package rows 20200618_a8524172-91fb-6eb2-e053-2a95a90a1cae.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 67046-335-30 67046033530 30 TABLET in 1 BLISTER PACK (67046-335-30) 30 tablet 2020-06-15 0000-00-00 No No Current