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Acyclovir
Acyclovir - 42291-109-50 - (Acyclovir)
Drug Information of Acyclovir
| Product NDC: | 42291-109 |
| Proprietary Name: | Acyclovir |
| Non Proprietary Name: | Acyclovir |
| Active Ingredient(s): | 800 mg/1 & nbsp; Acyclovir |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acyclovir
| Product NDC: | 42291-109 |
| Labeler Name: | AvKARE, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075382 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990305 |
Package Information of Acyclovir
| Package NDC: | 42291-109-50 |
| Package Description: | 500 TABLET in 1 BOTTLE (42291-109-50) |
NDC Information of Acyclovir
| NDC Code | 42291-109-50 |
| Proprietary Name | Acyclovir |
| Package Description | 500 TABLET in 1 BOTTLE (42291-109-50) |
| Product NDC | 42291-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acyclovir |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19990305 |
| Marketing Category Name | ANDA |
| Labeler Name | AvKARE, Inc. |
| Substance Name | ACYCLOVIR |
| Strength Number | 800 |
| 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] |
