Product Details for ANDA 040706
BENZTROPINE MESYLATE (BENZTROPINE MESYLATE)
0.5MG
Marketing Status: Discontinued
1MG
Marketing Status: Discontinued
2MG
Marketing Status: Discontinued
0.5MG
Marketing Status: Discontinued
Active Ingredient: BENZTROPINE MESYLATE
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 002
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
BENZTROPINE MESYLATE (BENZTROPINE MESYLATE)
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 0.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 002
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
1MG
Marketing Status: Discontinued
Active Ingredient: BENZTROPINE MESYLATE
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 003
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
BENZTROPINE MESYLATE (BENZTROPINE MESYLATE)
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 003
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
2MG
Marketing Status: Discontinued
Active Ingredient: BENZTROPINE MESYLATE
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 001
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: BENZTROPINE MESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040706
Product Number: 001
Approval Date: Feb 14, 2008
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status: Discontinued
Patent and Exclusivity Information