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] |