Active Ingredient: AMMONIUM CHLORIDE
Proprietary Name: AMMONIUM CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 3MEQ/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A086205
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: GD SEARLE LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information