Active Ingredient: ZOLPIDEM TARTRATE
Proprietary Name: ZOLPIDEM TARTRATE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 6.25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A213592
Product Number: 001
Approval Date: Jun 4, 2020
Applicant Holder Full Name: BRECKENRIDGE PHARMACEUTICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information