Details for New Drug Application (NDA): 019022
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NDA 019022 describes SODIUM CHLORIDE 5% IN PLASTIC CONTAINER, which is a drug marketed by B Braun and Baxter Hlthcare and is included in two NDAs. It is available from two suppliers. Additional details are available on the SODIUM CHLORIDE 5% IN PLASTIC CONTAINER profile page.
The generic ingredient in SODIUM CHLORIDE 5% IN PLASTIC CONTAINER is sodium chloride. There are one thousand four hundred and seventy-two drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the sodium chloride profile page.
The generic ingredient in SODIUM CHLORIDE 5% IN PLASTIC CONTAINER is sodium chloride. There are one thousand four hundred and seventy-two drug master file entries for this compound. Twenty-five suppliers are listed for this compound. Additional details are available on the sodium chloride profile page.
Summary for 019022
| Tradename: | SODIUM CHLORIDE 5% IN PLASTIC CONTAINER |
| Applicant: | Baxter Hlthcare |
| Ingredient: | sodium chloride |
| Patents: | 0 |
Pharmacology for NDA: 019022
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 019022
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| SODIUM CHLORIDE 3% IN PLASTIC CONTAINER | sodium chloride | INJECTABLE;INJECTION | 019022 | NDA | Baxter Healthcare Corporation | 0338-0054 | 0338-0054-03 | 24 BAG in 1 CARTON (0338-0054-03) / 500 mL in 1 BAG |
| SODIUM CHLORIDE 3% IN PLASTIC CONTAINER | sodium chloride | INJECTABLE;INJECTION | 019022 | NDA | Baxter Healthcare Corporation | 0338-0056 | 0338-0056-03 | 24 BAG in 1 CARTON (0338-0056-03) / 500 mL in 1 BAG |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 3GM/100ML | ||||
| Approval Date: | Nov 1, 1983 | TE: | AP | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 5GM/100ML | ||||
| Approval Date: | Nov 1, 1983 | TE: | AP | RLD: | Yes | ||||
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