Product NDC: | 60505-3247 |
Proprietary Name: | FAMCICLOVIR |
Non Proprietary Name: | FAMCICLOVIR |
Active Ingredient(s): | 500 mg/1 & nbsp; FAMCICLOVIR |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-3247 |
Labeler Name: | Apotex Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091480 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111220 |
Package NDC: | 60505-3247-3 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3247-3) |
NDC Code | 60505-3247-3 |
Proprietary Name | FAMCICLOVIR |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3247-3) |
Product NDC | 60505-3247 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FAMCICLOVIR |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111220 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp. |
Substance Name | FAMCICLOVIR |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | DNA Polymerase Inhibitors [MoA],DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient] |