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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 214184

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PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
225MG
Marketing Status: Prescription
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 225MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214184
Product Number: 001
Approval Date: Apr 21, 2021
Applicant Holder Full Name: ZYDUS WORLDWIDE DMCC
Marketing Status:  Prescription
Patent and Exclusivity Information
PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
325MG
Marketing Status: Prescription
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 325MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214184
Product Number: 002
Approval Date: Apr 21, 2021
Applicant Holder Full Name: ZYDUS WORLDWIDE DMCC
Marketing Status:  Prescription
Patent and Exclusivity Information
PROPAFENONE HYDROCHLORIDE (PROPAFENONE HYDROCHLORIDE)
425MG
Marketing Status: Prescription
Active Ingredient: PROPAFENONE HYDROCHLORIDE
Proprietary Name: PROPAFENONE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 425MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214184
Product Number: 003
Approval Date: Apr 21, 2021
Applicant Holder Full Name: ZYDUS WORLDWIDE DMCC
Marketing Status:  Prescription
Patent and Exclusivity Information
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