Product NDC: | 0378-4491 |
Proprietary Name: | Famciclovir |
Non Proprietary Name: | famciclovir |
Active Ingredient(s): | 250 mg/1 & nbsp; famciclovir |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0378-4491 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA201333 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130522 |
Package NDC: | 0378-4491-77 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4491-77) |
NDC Code | 0378-4491-77 |
Proprietary Name | Famciclovir |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4491-77) |
Product NDC | 0378-4491 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | famciclovir |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130522 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | FAMCICLOVIR |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient] |