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Acyclovir
Acyclovir - 68682-995-95 - (acyclovir)
Drug Information of Acyclovir
| Product NDC: | 68682-995 |
| Proprietary Name: | Acyclovir |
| Non Proprietary Name: | acyclovir |
| Active Ingredient(s): | 50 mg/g & nbsp; acyclovir |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acyclovir
| Product NDC: | 68682-995 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018604 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121003 |
Package Information of Acyclovir
| Package NDC: | 68682-995-95 |
| Package Description: | 1 TUBE in 1 CARTON (68682-995-95) > 30 g in 1 TUBE |
NDC Information of Acyclovir
| NDC Code | 68682-995-95 |
| Proprietary Name | Acyclovir |
| Package Description | 1 TUBE in 1 CARTON (68682-995-95) > 30 g in 1 TUBE |
| Product NDC | 68682-995 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acyclovir |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20121003 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | ACYCLOVIR |
| Strength Number | 50 |
| Strength Unit | mg/g |
| 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] |
