| NDC Code |
0121-0595-15 |
| Proprietary Name |
Sodium Citrate and Citric Acid |
| Package Description |
10 TRAY in 1 CASE (0121-0595-15) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE |
| Product NDC |
0121-0595 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
SODIUM CITRATE and CITRIC ACID MONOHYDRATE |
| Dosage Form Name |
SOLUTION |
| Route Name |
ORAL |
| Start Marketing Date |
19690101 |
| Marketing Category Name |
UNAPPROVED DRUG OTHER |
| Labeler Name |
Pharmaceutical Associates, Inc. |
| Substance Name |
CITRIC ACID MONOHYDRATE; SODIUM CITRATE |
| Strength Number |
334; 500 |
| Strength Unit |
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] |