Details for New Drug Application (NDA): 090343
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NDA 090343 describes LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER, which is a drug marketed by Baxter Hlthcare Corp, Eugia Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Hikma Farmaceutica, Hospira, Inforlife, and Knack, and is included in eight NDAs. It is available from eight suppliers. Additional details are available on the LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER profile page.
The generic ingredient in LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER is levofloxacin. There are thirty-one drug master file entries for this compound. Forty-six suppliers are listed for this compound. Additional details are available on the levofloxacin profile page.
The generic ingredient in LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER is levofloxacin. There are thirty-one drug master file entries for this compound. Forty-six suppliers are listed for this compound. Additional details are available on the levofloxacin profile page.
Summary for 090343
| Tradename: | LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER |
| Applicant: | Inforlife |
| Ingredient: | levofloxacin |
| Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 090343
Suppliers and Packaging for NDA: 090343
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER | levofloxacin | INJECTABLE;INJECTION | 090343 | ANDA | Hospira, Inc | 0409-2220 | 0409-2220-24 | 24 POUCH in 1 CARTON (0409-2220-24) / 1 BAG in 1 POUCH (0409-2220-01) / 50 mL in 1 BAG |
| LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER | levofloxacin | INJECTABLE;INJECTION | 090343 | ANDA | Hospira, Inc | 0409-3330 | 0409-3330-24 | 24 POUCH in 1 CARTON (0409-3330-24) / 1 BAG in 1 POUCH (0409-3330-01) / 100 mL in 1 BAG |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 250MG/50ML (EQ 5MG/ML) | ||||
| Approval Date: | Jul 7, 2011 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 500MG/100ML (EQ 5MG/ML) | ||||
| Approval Date: | Jul 7, 2011 | TE: | AP | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | EQ 750MG/150ML (EQ 5MG/ML) | ||||
| Approval Date: | Jul 7, 2011 | TE: | AP | RLD: | No | ||||
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