Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020771

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DETROL (TOLTERODINE TARTRATE)
1MG
Marketing Status: Prescription

Active Ingredient: TOLTERODINE TARTRATE
Proprietary Name: DETROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020771
Product Number: 001
Approval Date: Mar 25, 1998
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status:  Prescription
Patent and Exclusivity Information

DETROL (TOLTERODINE TARTRATE)
2MG
Marketing Status: Prescription

Active Ingredient: TOLTERODINE TARTRATE
Proprietary Name: DETROL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N020771
Product Number: 002
Approval Date: Mar 25, 1998
Applicant Holder Full Name: UPJOHN US 2 LLC
Marketing Status:  Prescription
Patent and Exclusivity Information