Balanced Salt is a Ophthalmic Solution in the Human Prescription Drug category. It is labeled and distributed by Akorn, Inc.. The primary component is Sodium Chloride; Potassium Chloride; Calcium Chloride; Magnesium Chloride; Sodium Acetate; Trisodium Citrate Dihydrate.
| Product ID | 17478-921_a9922ee0-385a-4abf-8fbc-0e60702bbc48 | 
| NDC | 17478-921 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Balanced Salt | 
| Generic Name | Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Acetate And Trisodium Citrate Dihydrate | 
| Dosage Form | Solution | 
| Route of Administration | OPHTHALMIC | 
| Marketing Start Date | 2014-11-27 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA075503 | 
| Labeler Name | Akorn, Inc. | 
| Substance Name | SODIUM CHLORIDE; POTASSIUM CHLORIDE; CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; SODIUM ACETATE; TRISODIUM CITRATE DIHYDRATE | 
| Active Ingredient Strength | 6 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL | 
| Pharm Classes | Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Acidifying Activity [MoA],Calculi Dissolution Agent [EPC],Anti-coagulant [EPC],Decreased Coagulation Factor Activity [PE],Calcium Chelating Activity [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2021-12-31 | 
| Marketing Start Date | 2014-11-27 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA075503 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2014-11-27 | 
| Ingredient | Strength | 
|---|---|
| SODIUM CHLORIDE | 6.4 mg/mL | 
| SPL SET ID: | eee80ec9-495f-413d-b3d6-03924e9d2a02 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0264-1945 | Balanced Salt | Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Acetate, and Sodium Citrate | 
| 0264-2514 | Balanced Salt | Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Acetate, and Sodium Citrate | 
| 17478-920 | BALANCED SALT | Calcium Chloride, Magnesium Chloride, Potassium Chloride, Sodium Acetate, Sodium Chloride, Sodium Citrate | 
| 17478-921 | Balanced Salt | Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Acetate and Trisodium Citrate Dihydrate |