Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 079141

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TOLTERODINE TARTRATE (TOLTERODINE TARTRATE)
2MG
Marketing Status: Prescription
Active Ingredient: TOLTERODINE TARTRATE
Proprietary Name: TOLTERODINE TARTRATE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079141
Product Number: 001
Approval Date: Nov 22, 2016
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:  Prescription
Patent and Exclusivity Information
TOLTERODINE TARTRATE (TOLTERODINE TARTRATE)
4MG
Marketing Status: Prescription
Active Ingredient: TOLTERODINE TARTRATE
Proprietary Name: TOLTERODINE TARTRATE
Dosage Form; Route of Administration: CAPSULE, EXTENDED RELEASE; ORAL
Strength: 4MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A079141
Product Number: 002
Approval Date: Nov 22, 2016
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:  Prescription
Patent and Exclusivity Information

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