Active Ingredient: BACLOFEN
Proprietary Name: KEMSTRO
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021589
Product Number: 001
Approval Date: Oct 30, 2003
Applicant Holder Full Name: UCB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: BACLOFEN
Proprietary Name: KEMSTRO
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021589
Product Number: 002
Approval Date: Oct 30, 2003
Applicant Holder Full Name: UCB INC
Marketing Status:
Discontinued
Patent and Exclusivity Information