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FORTAZ
FORTAZ - 0173-0382-37 - (ceftazidime)
Drug Information of FORTAZ
| Product NDC: | 0173-0382 |
| Proprietary Name: | FORTAZ |
| Non Proprietary Name: | ceftazidime |
| Active Ingredient(s): | 200 mg/mL & nbsp; ceftazidime |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FORTAZ
| Product NDC: | 0173-0382 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050578 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19891001 |
Package Information of FORTAZ
| Package NDC: | 0173-0382-37 |
| Package Description: | 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0173-0382-37) > 127 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of FORTAZ
| NDC Code | 0173-0382-37 |
| Proprietary Name | FORTAZ |
| Package Description | 6 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0173-0382-37) > 127 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 0173-0382 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ceftazidime |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19891001 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | CEFTAZIDIME SODIUM |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
