Product NDC: | 60505-0042 |
Proprietary Name: | ACYCLOVIR |
Non Proprietary Name: | ACYCLOVIR |
Active Ingredient(s): | 200 mg/1 & nbsp; ACYCLOVIR |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-0042 |
Labeler Name: | Apotex Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075677 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060320 |
Package NDC: | 60505-0042-5 |
Package Description: | 500 CAPSULE in 1 BOTTLE (60505-0042-5) |
NDC Code | 60505-0042-5 |
Proprietary Name | ACYCLOVIR |
Package Description | 500 CAPSULE in 1 BOTTLE (60505-0042-5) |
Product NDC | 60505-0042 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ACYCLOVIR |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20060320 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp. |
Substance Name | ACYCLOVIR |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical 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 [Chemical/Ingredient] |