Product Details for ANDA 206890
ILOPERIDONE (ILOPERIDONE)
1MG
Marketing Status: Discontinued
2MG
Marketing Status: Discontinued
4MG
Marketing Status: Discontinued
6MG
Marketing Status: Discontinued
8MG
Marketing Status: Discontinued
10MG
Marketing Status: Discontinued
12MG
Marketing Status: Discontinued
1MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 001
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 001
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
2MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 002
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 002
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
4MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 003
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 003
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
6MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 6MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 004
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 6MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 004
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
8MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 005
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 005
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 006
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
ILOPERIDONE (ILOPERIDONE)
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 006
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
12MG
Marketing Status: Discontinued
Active Ingredient: ILOPERIDONE
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 007
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ILOPERIDONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 12MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A206890
Product Number: 007
Approval Date: May 5, 2022
Applicant Holder Full Name: LUPIN LTD
Marketing Status: Discontinued
Patent and Exclusivity Information