Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations
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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "022192."



Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 1MG
Application Number: N022192
Product Number: 001
Approval Date: May 6, 2009
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 2MG
Application Number: N022192
Product Number: 002
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 4MG
Application Number: N022192
Product Number: 003
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 6MG
Application Number: N022192
Product Number: 004
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 8MG
Application Number: N022192
Product Number: 005
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 10MG
Application Number: N022192
Product Number: 006
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

Active Ingredient: ILOPERIDONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: FANAPT
Applicant: NOVARTIS
Strength: 12MG
Application Number: N022192
Product Number: 007
Approval Date: May 6, 2009
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code:
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through March 01, 2014
Patent and Generic Drug Product Data Last Updated April 18, 2014

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