Home NDC 10544-089 Acyclovir
Product NDC 10544-089
11-digit product format 105440089
Labeler code 10544
Product ID 10544-089_f41aa20a-8824-477e-8f04-69760ba1197e
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Blenheim Pharmacal, Inc.
Application ANDA074975
Marketing category ANDA
Marketing start 2012-10-24
Marketing end 0000-00-00
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 E
Listing certified through 2017-12-31
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 10544-089-25 Acyclovir 25 in 1 BOTTLE CAPSULE 25 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10544-089 ACYCLOVIR CAPSULE ACYCLOVIR TABLET [BLENHEIM PHARMACAL, INC.] 1 Legacy NDC, 1 package rows 20160609_f41aa20a-8824-477e-8f04-69760ba1197e.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 10544-089-25 10544008925 25 in 1 BOTTLE Historical