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Cefazolin
Cefazolin - 0338-3503-41 - (Cefazolin Sodium)
Drug Information of Cefazolin
| Product NDC: | 0338-3503 |
| Proprietary Name: | Cefazolin |
| Non Proprietary Name: | Cefazolin Sodium |
| Active Ingredient(s): | 1 g/50mL & nbsp; Cefazolin Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefazolin
| Product NDC: | 0338-3503 |
| Labeler Name: | Baxter Healthcare Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063002 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19910328 |
Package Information of Cefazolin
| Package NDC: | 0338-3503-41 |
| Package Description: | 24 BAG in 1 CASE (0338-3503-41) > 50 mL in 1 BAG |
NDC Information of Cefazolin
| NDC Code | 0338-3503-41 |
| Proprietary Name | Cefazolin |
| Package Description | 24 BAG in 1 CASE (0338-3503-41) > 50 mL in 1 BAG |
| Product NDC | 0338-3503 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefazolin Sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19910328 |
| Marketing Category Name | ANDA |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | CEFAZOLIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
