Details for New Drug Application (NDA): 018016
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The generic ingredient in SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER is sodium chloride. There are one thousand four hundred and seventy-two drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the sodium chloride profile page.
Summary for 018016
| Tradename: | SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER |
| Applicant: | Baxter Hlthcare |
| Ingredient: | sodium chloride |
| Patents: | 0 |
Pharmacology for NDA: 018016
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 018016
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER | sodium chloride | INJECTABLE;INJECTION | 018016 | NDA | Baxter Healthcare Corporation | 0338-0043 | 0338-0043-03 | 500 mL in 1 BAG (0338-0043-03) |
| SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER | sodium chloride | INJECTABLE;INJECTION | 018016 | NDA | Baxter Healthcare Corporation | 0338-0043 | 0338-0043-04 | 1000 mL in 1 BAG (0338-0043-04) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 450MG/100ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AP | RLD: | Yes | ||||
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