Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020850

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MICARDIS (TELMISARTAN)
20MG Marketing Status: Prescription

Active Ingredient: TELMISARTAN
Proprietary Name: MICARDIS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020850
Product Number: 003
Approval Date: Apr 4, 2000
Applicant Holder Full Name: BOEHRINGER INGELHEIM
Marketing Status:  Prescription
Patent and Exclusivity Information

MICARDIS (TELMISARTAN)
40MG Marketing Status: Prescription

Active Ingredient: TELMISARTAN
Proprietary Name: MICARDIS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020850
Product Number: 001
Approval Date: Nov 10, 1998
Applicant Holder Full Name: BOEHRINGER INGELHEIM
Marketing Status:  Prescription
Patent and Exclusivity Information

MICARDIS (TELMISARTAN)
80MG Marketing Status: Prescription

Active Ingredient: TELMISARTAN
Proprietary Name: MICARDIS
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 80MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N020850
Product Number: 002
Approval Date: Nov 10, 1998
Applicant Holder Full Name: BOEHRINGER INGELHEIM
Marketing Status:  Prescription
Patent and Exclusivity Information

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