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Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 20MEQ/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A214892
Product Number: 001
Approval Date: Dec 30, 2022
Applicant Holder Full Name: ANDA REPOSITORY LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: POTASSIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 40MEQ/15ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A214892
Product Number: 002
Approval Date: Dec 30, 2022
Applicant Holder Full Name: ANDA REPOSITORY LLC
Marketing Status:
Prescription
Patent and Exclusivity Information