Active Ingredient: AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE
Proprietary Name: CHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 25MG BASE;10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070766
Product Number: 001
Approval Date: Dec 10, 1986
Applicant Holder Full Name: ANDA REPOSITORY LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
