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Acyclovir
Acyclovir - 51079-448-20 - (acyclovir)
Drug Information of Acyclovir
| Product NDC: | 51079-448 |
| Proprietary Name: | Acyclovir |
| Non Proprietary Name: | acyclovir |
| Active Ingredient(s): | 400 mg/1 & nbsp; acyclovir |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acyclovir
| Product NDC: | 51079-448 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075211 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100723 |
Package Information of Acyclovir
| Package NDC: | 51079-448-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-448-20) > 1 TABLET in 1 BLISTER PACK (51079-448-01) |
NDC Information of Acyclovir
| NDC Code | 51079-448-20 |
| Proprietary Name | Acyclovir |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-448-20) > 1 TABLET in 1 BLISTER PACK (51079-448-01) |
| Product NDC | 51079-448 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acyclovir |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20100723 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | ACYCLOVIR |
| Strength Number | 400 |
| 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] |
