Details for New Drug Application (NDA): 022417

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NDA 022417 describes NORVIR, which is a drug marketed by Abbott and Abbvie and is included in five NDAs. It is available from one supplier. Additional details are available on the NORVIR profile page.

The generic ingredient in NORVIR is ritonavir. There are twenty-one drug master file entries for this compound. Seven 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

Pharmacology for NDA: 022417

Mechanism of Action	Breast Cancer Resistance Protein Inhibitors Cytochrome P450 1A2 Inducers Cytochrome P450 2B6 Inducers Cytochrome P450 2C19 Inducers Cytochrome P450 2C9 Inducers Cytochrome P450 2D6 Inhibitors Cytochrome P450 3A Inducers Cytochrome P450 3A Inhibitors Cytochrome P450 3A4 Inhibitors HIV Protease Inhibitors P-Glycoprotein Inhibitors UDP Glucuronosyltransferases Inducers

Medical Subject Heading (MeSH) Categories for 022417

Cytochrome P-450 CYP3A Inhibitors
HIV Protease Inhibitors

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

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Abbvie	NORVIR	ritonavir	TABLET;ORAL	022417-001	Feb 10, 2010	⤷ Subscribe	⤷ Subscribe
Abbvie	NORVIR	ritonavir	TABLET;ORAL	022417-001	Feb 10, 2010	⤷ Subscribe	⤷ Subscribe
Abbvie	NORVIR	ritonavir	TABLET;ORAL	022417-001	Feb 10, 2010	⤷ Subscribe	⤷ Subscribe
Abbvie	NORVIR	ritonavir	TABLET;ORAL	022417-001	Feb 10, 2010	⤷ Subscribe	⤷ Subscribe
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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