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Active Ingredient: ISOSORBIDE MONONITRATE
Proprietary Name: ISOSORBIDE MONONITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075037
Product Number: 002
Approval Date: Oct 30, 1998
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: ISOSORBIDE MONONITRATE
Proprietary Name: ISOSORBIDE MONONITRATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A075037
Product Number: 001
Approval Date: Oct 30, 1998
Applicant Holder Full Name: ACTAVIS ELIZABETH LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
