Active Ingredient: BETHANECHOL CHLORIDE
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084712
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: LANNETT CO INC
Marketing Status:
Discontinued
Patent and Exclusivity Information