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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 "014399."



Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 25MG
Application Number: N014399
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 50MG
Application Number: N014399
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 75MG
Application Number: N014399
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 100MG
Application Number: N014399
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 150MG
Application Number: N014399
Product Number: 006
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: DESIPRAMINE HYDROCHLORIDE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: NORPRAMIN
Applicant: SANOFI AVENTIS US
Strength: 10MG
Application Number: N014399
Product Number: 007
Approval Date: Feb 11, 1982
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
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 September 2014
Patent and Generic Drug Product Data Last Updated October 29, 2014

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