Active Ingredient: AMMONIUM CHLORIDE
Proprietary Name: AMMONIUM CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5MEQ/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A083130
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status:
Discontinued
Patent and Exclusivity Information