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AZACTAM
AZACTAM - 0003-2570-16 - (AZTREONAM)
Drug Information of AZACTAM
| Product NDC: | 0003-2570 |
| Proprietary Name: | AZACTAM |
| Non Proprietary Name: | AZTREONAM |
| Active Ingredient(s): | 2 g/1 & nbsp; AZTREONAM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AZACTAM
| Product NDC: | 0003-2570 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050580 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100401 |
Package Information of AZACTAM
| Package NDC: | 0003-2570-16 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0003-2570-16) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
NDC Information of AZACTAM
| NDC Code | 0003-2570-16 |
| Proprietary Name | AZACTAM |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0003-2570-16) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0003-2570 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AZTREONAM |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; 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/1 |
| Pharmaceutical Classes | Monobactam Antibacterial [EPC],Monobactams [Chemical/Ingredient] |
