| Product NDC: | 0003-2240 |
| Proprietary Name: | AZACTAM |
| Non Proprietary Name: | AZTREONAM |
| Active Ingredient(s): | 2 g/50mL & nbsp; AZTREONAM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0003-2240 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050632 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100401 |
| Package NDC: | 0003-2240-11 |
| Package Description: | 24 CONTAINER in 1 PACKAGE (0003-2240-11) > 50 mL in 1 CONTAINER |
| NDC Code | 0003-2240-11 |
| Proprietary Name | AZACTAM |
| Package Description | 24 CONTAINER in 1 PACKAGE (0003-2240-11) > 50 mL in 1 CONTAINER |
| Product NDC | 0003-2240 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AZTREONAM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | AZTREONAM |
| Strength Number | 2 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Monobactam Antibacterial [EPC],Monobactams [Chemical/Ingredient] |