Home NDC 50090-0644 Acyclovir
Product NDC 50090-0644
11-digit product format 500900644
Labeler code 50090
Product ID 50090-0644_0c62fccb-8ff3-4079-8661-0b5bf292f0f7
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler A-S Medication Solutions
Application ANDA075382
Marketing category ANDA
Marketing start 2009-10-22
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 Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 50090-0644-2 50090064402 25 TABLET in 1 BOTTLE (50090-0644-2) 25 tablet 2014-11-28 0000-00-00 No No Current 50090-0644-3 50090064403 50 TABLET in 1 BOTTLE (50090-0644-3) 50 tablet 2014-11-28 0000-00-00 No No Current 50090-0644-4 50090064404 15 TABLET in 1 BOTTLE (50090-0644-4) 15 tablet 2014-11-28 0000-00-00 No No Current 50090-0644-5 50090064405 30 TABLET in 1 BOTTLE (50090-0644-5) 30 tablet 2014-11-28 0000-00-00 No No Current 50090-0644-6 50090064406 60 TABLET in 1 BOTTLE (50090-0644-6) 60 tablet 2014-11-28 0000-00-00 No No Current 50090-0644-9 50090064409 45 TABLET in 1 BOTTLE (50090-0644-9) 45 tablet 2014-11-28 0000-00-00 No No Current