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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 078992

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DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
5MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 001
Approval Date: Nov 23, 2021
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
10MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 002
Approval Date: Nov 23, 2021
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
15MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 15MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 003
Approval Date: Nov 18, 2013
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
30MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 004
Approval Date: Nov 18, 2013
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
20MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 005
Approval Date: Nov 23, 2021
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
DEXMETHYLPHENIDATE HYDROCHLORIDE (DEXMETHYLPHENIDATE HYDROCHLORIDE)
40MG
Marketing Status: Prescription
Active Ingredient: DEXMETHYLPHENIDATE HYDROCHLORIDE
Proprietary Name: DEXMETHYLPHENIDATE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078992
Product Number: 006
Approval Date: Nov 23, 2021
Applicant Holder Full Name: INTELLIPHARMACEUTICS CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
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