Active Ingredient: PROCYCLIDINE HYDROCHLORIDE
Proprietary Name: KEMADRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 2MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N009818
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MONARCH PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: PROCYCLIDINE HYDROCHLORIDE
Proprietary Name: KEMADRIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N009818
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: MONARCH PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information