Details for New Drug Application (NDA): 022417
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The generic ingredient in NORVIR is ritonavir. There are twenty-one drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the ritonavir profile page.
Summary for 022417
Tradename: | NORVIR |
Applicant: | Abbvie |
Ingredient: | ritonavir |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 022417
Medical Subject Heading (MeSH) Categories for 022417
Suppliers and Packaging for NDA: 022417
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
NORVIR | ritonavir | TABLET;ORAL | 022417 | NDA | AbbVie Inc. | 0074-2340 | 0074-2340-30 | 30 TABLET, FILM COATED in 1 BOTTLE (0074-2340-30) |
NORVIR | ritonavir | TABLET;ORAL | 022417 | NDA | AbbVie Inc. | 0074-3333 | 0074-3333-30 | 30 TABLET, FILM COATED in 1 BOTTLE (0074-3333-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Feb 10, 2010 | TE: | AB | RLD: | Yes |
Expired US Patents for NDA 022417
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Patent No. | Patent Expiration |
---|---|---|---|---|---|---|---|
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
Abbvie | NORVIR | ritonavir | TABLET;ORAL | 022417-001 | Feb 10, 2010 | ⤷ Try a Trial | ⤷ Try a Trial |
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >Patent No. | >Patent Expiration |
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