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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 "020747."



Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 0.2MG BASE
Application Number: N020747
Product Number: 001
Approval Date: Nov 4, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 0.4MG BASE
Application Number: N020747
Product Number: 002
Approval Date: Nov 4, 1998
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 0.6MG BASE
Application Number: N020747
Product Number: 003
Approval Date: Nov 4, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 0.8MG BASE
Application Number: N020747
Product Number: 004
Approval Date: Nov 4, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 1.2MG BASE
Application Number: N020747
Product Number: 005
Approval Date: Nov 4, 1998
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB
Patent and Exclusivity Info for this product: View

Active Ingredient: FENTANYL CITRATE
Dosage Form;Route: TROCHE/LOZENGE;TRANSMUCOSAL
Proprietary Name: ACTIQ
Applicant: CEPHALON
Strength: EQ 1.6MG BASE
Application Number: N020747
Product Number: 006
Approval Date: Nov 4, 1998
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 July 2014
Patent and Generic Drug Product Data Last Updated August 26, 2014

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