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Acyclovir
Acyclovir - 21695-011-35 - (acyclovir)
Drug Information of Acyclovir
| Product NDC: | 21695-011 |
| 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: | 21695-011 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA074980 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19981030 |
Package Information of Acyclovir
| Package NDC: | 21695-011-35 |
| Package Description: | 35 TABLET in 1 BOTTLE (21695-011-35) |
NDC Information of Acyclovir
| NDC Code | 21695-011-35 |
| Proprietary Name | Acyclovir |
| Package Description | 35 TABLET in 1 BOTTLE (21695-011-35) |
| Product NDC | 21695-011 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acyclovir |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19981030 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Rebel Distributors Corp |
| 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] |
