Details for New Drug Application (NDA): 020734
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NDA 020734 describes CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER, which is a drug marketed by Baxter Hlthcare and is included in one NDA. It is available from one supplier. Additional details are available on the CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER profile page.
The generic ingredient in CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER is amino acids; dextrose. There are three hundred and fifty drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the amino acids; dextrose profile page.
The generic ingredient in CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER is amino acids; dextrose. There are three hundred and fifty drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the amino acids; dextrose profile page.
Summary for 020734
| Tradename: | CLINIMIX 8/14 SULFITE FREE IN DEXTROSE 14% IN PLASTIC CONTAINER |
| Applicant: | Baxter Hlthcare |
| Ingredient: | amino acids; dextrose |
| Patents: | 0 |
Suppliers and Packaging for NDA: 020734
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CLINIMIX 2.75/10 SULFITE FREE IN DEXTROSE 10% IN PLASTIC CONTAINER | amino acids; dextrose | INJECTABLE;INJECTION | 020734 | NDA | Baxter Healthcare Corporation | 0338-0180 | 0338-0180-06 | 6 BAG in 1 CARTON (0338-0180-06) / 1000 mL in 1 BAG (0338-0180-01) |
| CLINIMIX 2.75/10 SULFITE FREE IN DEXTROSE 10% IN PLASTIC CONTAINER | amino acids; dextrose | INJECTABLE;INJECTION | 020734 | NDA | Baxter Healthcare Corporation | 0338-0184 | 0338-0184-04 | 4 BAG in 1 CARTON (0338-0184-04) / 2000 mL in 1 BAG (0338-0184-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2.75%;5GM/100ML | ||||
| Approval Date: | Sep 29, 1997 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2.75%;10GM/100ML | ||||
| Approval Date: | Sep 29, 1997 | TE: | RLD: | No | |||||
Profile for product number 005
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2.75%;25GM/100ML | ||||
| Approval Date: | Sep 29, 1997 | TE: | RLD: | No | |||||
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