Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 076418

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AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
EQ 2.5MG BASE
Marketing Status: Discontinued

Active Ingredient: AMLODIPINE BESYLATE
Proprietary Name: AMLODIPINE BESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2.5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076418
Product Number: 001
Approval Date: Oct 3, 2005
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
EQ 5MG BASE
Marketing Status: Discontinued

Active Ingredient: AMLODIPINE BESYLATE
Proprietary Name: AMLODIPINE BESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076418
Product Number: 002
Approval Date: Oct 3, 2005
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
EQ 10MG BASE
Marketing Status: Discontinued

Active Ingredient: AMLODIPINE BESYLATE
Proprietary Name: AMLODIPINE BESYLATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 10MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076418
Product Number: 003
Approval Date: Oct 3, 2005
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information