Active Ingredient: CHLORDIAZEPOXIDE HYDROCHLORIDE
Proprietary Name: CHLORDIAZEPOXIDE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084598
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information