Details for New Drug Application (NDA): 019904
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NDA 019904 describes POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER, which is a drug marketed by Baxter Hlthcare and Icu Medical Inc and is included in two NDAs. It is available from two suppliers. Additional details are available on the POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER profile page.
The generic ingredient in POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER is potassium chloride. There are two hundred and forty drug master file entries for this compound. Eighty-seven suppliers are listed for this compound. Additional details are available on the potassium chloride profile page.
The generic ingredient in POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER is potassium chloride. There are two hundred and forty drug master file entries for this compound. Eighty-seven suppliers are listed for this compound. Additional details are available on the potassium chloride profile page.
Summary for 019904
| Tradename: | POTASSIUM CHLORIDE 40MEQ IN PLASTIC CONTAINER |
| Applicant: | Baxter Hlthcare |
| Ingredient: | potassium chloride |
| Patents: | 0 |
Pharmacology for NDA: 019904
| Mechanism of Action | Osmotic Activity |
| Physiological Effect | Increased Large Intestinal Motility Inhibition Large Intestine Fluid/Electrolyte Absorption |
Suppliers and Packaging for NDA: 019904
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| POTASSIUM CHLORIDE 10MEQ IN PLASTIC CONTAINER | potassium chloride | INJECTABLE;INJECTION | 019904 | NDA | Baxter Healthcare Corporation | 0338-0703 | 0338-0703-41 | 24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG |
| POTASSIUM CHLORIDE 20MEQ IN PLASTIC CONTAINER | potassium chloride | INJECTABLE;INJECTION | 019904 | NDA | Baxter Healthcare Corporation | 0338-0703 | 0338-0703-41 | 24 BAG in 1 CARTON (0338-0703-41) / 50 mL in 1 BAG |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 14.9MG/ML | ||||
| Approval Date: | Dec 26, 1989 | TE: | AP | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 29.8MG/ML | ||||
| Approval Date: | Dec 26, 1989 | TE: | AP | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2.24GM/100ML | ||||
| Approval Date: | Dec 26, 1989 | TE: | RLD: | Yes | |||||
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