Active Ingredient: DOXEPIN HYDROCHLORIDE
Proprietary Name: DOXEPIN HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 3MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A214823
Product Number: 001
Approval Date: Apr 3, 2023
Applicant Holder Full Name: MSN LABORATORIES PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information