Active Ingredient: NOREPINEPHRINE BITARTRATE
Proprietary Name: NOREPINEPHRINE BITARTRATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 1MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A211980
Product Number: 001
Approval Date: Jan 29, 2021
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information