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