Search results from the "OB_Rx" table for query
on "020363."
| Active Ingredient: | FAMCICLOVIR |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | FAMVIR |
| Applicant: | NOVARTIS |
| Strength: | 250MG |
| Application Number: | 020363 |
| Product Number: | 001 |
| Approval Date: | Apr 26, 1996 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | FAMCICLOVIR |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | FAMVIR |
| Applicant: | NOVARTIS |
| Strength: | 500MG |
| Application Number: | 020363 |
| Product Number: | 002 |
| Approval Date: | Jun 29, 1994 |
| Reference Listed Drug | Yes |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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| Active Ingredient: | FAMCICLOVIR |
| Dosage Form;Route: | TABLET; ORAL |
| Proprietary Name: | FAMVIR |
| Applicant: | NOVARTIS |
| Strength: | 125MG |
| Application Number: | 020363 |
| Product Number: | 003 |
| Approval Date: | Dec 11, 1995 |
| Reference Listed Drug | No |
| RX/OTC/DISCN: | RX |
| TE Code: | AB |
| Patent and Exclusivity Info for this product: | View |
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| Office of Generic Drugs |
| Division of Labeling and Program Support |
| Update Frequency: |
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| Generic Drug Product Information & Patent Information - Daily |
| Orange Book Data Updated Through October, 2009 |
| Patent and Generic Drug Product Data Last Updated: November 20, 2009 |