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TRICITRATES - 0121-0677-16 - (POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE)

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Drug Information of TRICITRATES

Product NDC: 0121-0677
Proprietary Name: TRICITRATES
Non Proprietary Name: POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE
Active Ingredient(s): 334; 550; 500    mg/5mL; mg/5mL; mg/5mL & nbsp;   POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of TRICITRATES

Product NDC: 0121-0677
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050525

Package Information of TRICITRATES

Package NDC: 0121-0677-16
Package Description: 473 mL in 1 BOTTLE (0121-0677-16)

NDC Information of TRICITRATES

NDC Code 0121-0677-16
Proprietary Name TRICITRATES
Package Description 473 mL in 1 BOTTLE (0121-0677-16)
Product NDC 0121-0677
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20050525
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Pharmaceutical Associates, Inc.
Substance Name CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE
Strength Number 334; 550; 500
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA]

Complete Information of TRICITRATES


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