Home NDC 68382-992 acyclovir
Product NDC 68382-992
11-digit product format 683820992
Labeler code 68382
Product ID 68382-992_ab5bf4c6-9400-4131-bb40-f172c424ac93
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name acyclovir
Dosage form OINTMENT
Route TOPICAL
Labeler Zydus Pharmaceuticals (USA) Inc.
Application ANDA205974
Marketing category ANDA
Marketing start 2019-03-21
Marketing end 2022-05-31
Substance ACYCLOVIR
Active strength 50 mg/g
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 0000-00-00
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 68382-992-01 68382099201 1 TUBE in 1 CARTON (68382-992-01) > 15 g in 1 TUBE 1 tube 2019-03-21 0000-00-00 No No Current 68382-992-04 68382099204 1 TUBE in 1 CARTON (68382-992-04) > 30 g in 1 TUBE 1 tube 2019-03-21 0000-00-00 No No Current