Home NDC 16714-668 Acyclovir
Product NDC 16714-668
11-digit product format 167140668
Labeler code 16714
Product ID 16714-668_aa103e4a-186c-4e00-9205-95a2a32f9ba1
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Acyclovir
Dosage form OINTMENT
Route TOPICAL
Labeler NorthStar Rx LLC
Application ANDA204605
Marketing category ANDA
Marketing start 2014-01-03
Marketing end 0000-00-00
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 2021-12-31
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 16714-668-01 16714066801 1 TUBE in 1 CARTON (16714-668-01) > 15 g in 1 TUBE 1 tube 2014-01-03 0000-00-00 No No Current 16714-668-02 16714066802 1 TUBE in 1 CARTON (16714-668-02) > 30 g in 1 TUBE 1 tube 2014-01-03 0000-00-00 No No Current