Home NDC 71335-1111 Acyclovir
Product NDC 71335-1111
11-digit product format 713351111
Labeler code 71335
Product ID 71335-1111_9169d63d-a8fc-461d-9f66-27b3e4db3237
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form TABLET
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA210401
Marketing category ANDA
Marketing start 2018-05-04
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 71335-1111-1 71335111101 25 TABLET in 1 BOTTLE (71335-1111-1) 25 tablet 2019-02-26 0000-00-00 No No Current 71335-1111-2 71335111102 30 TABLET in 1 BOTTLE (71335-1111-2) 30 tablet 2019-02-26 0000-00-00 No No Current 71335-1111-3 71335111103 100 TABLET in 1 BOTTLE (71335-1111-3) 100 tablet 2019-02-26 0000-00-00 No No Current 71335-1111-4 71335111104 300 TABLET in 1 BOTTLE (71335-1111-4) 300 tablet 2019-02-26 0000-00-00 No No Current 71335-1111-5 71335111105 500 TABLET in 1 BOTTLE (71335-1111-5) 500 tablet 2019-02-26 0000-00-00 No No Current