Details for New Drug Application (NDA): 017378
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The generic ingredient in PLASMA-LYTE A IN PLASTIC CONTAINER is magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium gluconate. There are one hundred and forty-six drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium gluconate profile page.
Summary for 017378
| Tradename: | PLASMA-LYTE A IN PLASTIC CONTAINER |
| Applicant: | Baxter Hlthcare |
| Ingredient: | magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium gluconate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 017378
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINER | magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium gluconate | INJECTABLE;INJECTION | 017378 | NDA | Baxter Healthcare Corporation | 0338-0221 | 0338-0221-03 | 500 mL in 1 BAG (0338-0221-03) |
| PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINER | magnesium chloride; potassium chloride; sodium acetate; sodium chloride; sodium gluconate | INJECTABLE;INJECTION | 017378 | NDA | Baxter Healthcare Corporation | 0338-0221 | 0338-0221-04 | 1000 mL in 1 BAG (0338-0221-04) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML | ||||
| Approval Date: | Approved Prior to Jan 1, 1982 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML | ||||
| Approval Date: | Nov 22, 1982 | TE: | AP | RLD: | Yes | ||||
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