Details for New Drug Application (NDA): 018826
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NDA 018826 describes DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER, which is a drug marketed by Baxter Hlthcare and Hospira and is included in two NDAs. It is available from four suppliers. Additional details are available on the DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER profile page.
The generic ingredient in DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER is dopamine hydrochloride. There are nine drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.
The generic ingredient in DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER is dopamine hydrochloride. There are nine drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.
Summary for 018826
| Tradename: | DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER |
| Applicant: | Hospira |
| Ingredient: | dopamine hydrochloride |
| Patents: | 0 |
Suppliers and Packaging for NDA: 018826
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER | dopamine hydrochloride | INJECTABLE;INJECTION | 018826 | NDA | Hospira, Inc. | 0409-0042 | 0409-0042-12 | 12 POUCH in 1 CASE (0409-0042-12) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-0042-01) |
| DOPAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER | dopamine hydrochloride | INJECTABLE;INJECTION | 018826 | NDA | Hospira, Inc. | 0409-1858 | 0409-1858-12 | 12 POUCH in 1 CASE (0409-1858-12) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-1858-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 80MG/100ML | ||||
| Approval Date: | Sep 30, 1983 | TE: | AP | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 160MG/100ML | ||||
| Approval Date: | Sep 30, 1983 | TE: | AP | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 320MG/100ML | ||||
| Approval Date: | Sep 30, 1983 | TE: | AP | RLD: | Yes | ||||
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