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Viramune
Viramune - 53808-0808-1 - (nevirapine)
Drug Information of Viramune
| Product NDC: | 53808-0808 |
| Proprietary Name: | Viramune |
| Non Proprietary Name: | nevirapine |
| Active Ingredient(s): | 200 mg/1 & nbsp; nevirapine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Viramune
| Product NDC: | 53808-0808 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020636 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090701 |
Package Information of Viramune
| Package NDC: | 53808-0808-1 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (53808-0808-1) |
NDC Information of Viramune
| NDC Code | 53808-0808-1 |
| Proprietary Name | Viramune |
| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0808-1) |
| Product NDC | 53808-0808 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nevirapine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | NDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | NEVIRAPINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Non-Nucleoside Analog [Chemical/Ingredient],Non-Nucleoside Reverse Transcriptase Inhibitors [MoA] |
