Details for New Drug Application (NDA): 020309
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NDA 020309 describes MAGNESIUM SULFATE IN PLASTIC CONTAINER, which is a drug marketed by Amneal, Baxter Hlthcare Corp, Fresenius Kabi Usa, Gland, Hospira, Hq Spclt Pharma, Milla Pharms, and Mylan Labs Ltd, and is included in eight NDAs. It is available from twelve suppliers. Additional details are available on the MAGNESIUM SULFATE IN PLASTIC CONTAINER profile page.
The generic ingredient in MAGNESIUM SULFATE IN PLASTIC CONTAINER is magnesium sulfate. There is one drug master file entry for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the magnesium sulfate profile page.
The generic ingredient in MAGNESIUM SULFATE IN PLASTIC CONTAINER is magnesium sulfate. There is one drug master file entry for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the magnesium sulfate profile page.
Summary for 020309
| Tradename: | MAGNESIUM SULFATE IN PLASTIC CONTAINER |
| Applicant: | Hospira |
| Ingredient: | magnesium sulfate |
| Patents: | 0 |
Suppliers and Packaging for NDA: 020309
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | magnesium sulfate | INJECTABLE;INJECTION | 020309 | NDA | Hospira, Inc. | 0409-2050 | 0409-2050-20 | 20 POUCH in 1 CASE (0409-2050-20) / 1 BAG in 1 POUCH / 500 mL in 1 BAG (0409-2050-01) |
| MAGNESIUM SULFATE IN PLASTIC CONTAINER | magnesium sulfate | INJECTABLE;INJECTION | 020309 | NDA | Hospira, Inc. | 0409-3164 | 0409-3164-12 | 12 POUCH in 1 CASE (0409-3164-12) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG (0409-3164-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 4GM/100ML (40MG/ML) | ||||
| Approval Date: | Jun 24, 1994 | TE: | AP | RLD: | Yes | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 4GM/50ML (80MG/ML) | ||||
| Approval Date: | Jun 24, 1994 | TE: | AP | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 2GM/50ML (40MG/ML) | ||||
| Approval Date: | Jan 26, 2007 | TE: | AP | RLD: | Yes | ||||
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