Home NDC 63629-7636 Acyclovir
Product NDC 63629-7636
11-digit product format 636297636
Labeler code 63629
Product ID 63629-7636_2fd60137-17d0-4669-89cf-727c58551413
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form CAPSULE
Route ORAL
Labeler Bryant Ranch Prepack
Application ANDA206261
Marketing category ANDA
Marketing start 2017-08-17
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 2021-12-31
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 63629-7636-1 63629763601 30 CAPSULE in 1 BOTTLE (63629-7636-1) 30 capsule 2018-08-15 0000-00-00 No No Current 63629-7636-2 63629763602 60 CAPSULE in 1 BOTTLE (63629-7636-2) 60 capsule 2018-08-15 0000-00-00 No No Current 63629-7636-3 63629763603 100 CAPSULE in 1 BOTTLE (63629-7636-3) 100 capsule 2018-08-15 0000-00-00 No No Current 63629-7636-4 63629763604 300 CAPSULE in 1 BOTTLE (63629-7636-4) 300 capsule 2018-08-15 0000-00-00 No No Current 63629-7636-5 63629763605 500 CAPSULE in 1 BOTTLE (63629-7636-5) 500 capsule 2018-08-15 0000-00-00 No No Current