Home NDC 70518-2496 ACYCLOVIR
Product NDC 70518-2496
11-digit product format 705182496
Labeler code 70518
Product ID 70518-2496_d04bf5bd-4aa8-ec42-e053-2995a90a42c8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form CAPSULE
Route ORAL
Labeler REMEDYREPACK INC.
Application ANDA074889
Marketing category ANDA
Marketing start 2019-12-18
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 No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70518-2496-0 70518249600 30 CAPSULE in 1 BLISTER PACK (70518-2496-0) 30 capsule 2019-12-18 0000-00-00 No No Current 70518-2496-1 70518249601 30 CAPSULE in 1 BLISTER PACK (70518-2496-1) 30 capsule 2021-10-15 0000-00-00 No No Current