Active Ingredient: GLYBURIDE
Proprietary Name: GLYBURIDE (MICRONIZED)
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 1.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075174
Product Number: 001
Approval Date: Jun 22, 1998
Applicant Holder Full Name: CHARTWELL RX SCIENCES LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
