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Cefazolin
Cefazolin - 63323-238-61 - (Cefazolin Sodium)
Drug Information of Cefazolin
| Product NDC: | 63323-238 |
| Proprietary Name: | Cefazolin |
| Non Proprietary Name: | Cefazolin Sodium |
| Active Ingredient(s): | 10 g/1 & nbsp; Cefazolin Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefazolin
| Product NDC: | 63323-238 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065306 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110614 |
Package Information of Cefazolin
| Package NDC: | 63323-238-61 |
| Package Description: | 10 VIAL in 1 CARTON (63323-238-61) > 1 POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of Cefazolin
| NDC Code | 63323-238-61 |
| Proprietary Name | Cefazolin |
| Package Description | 10 VIAL in 1 CARTON (63323-238-61) > 1 POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 63323-238 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefazolin Sodium |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110614 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFAZOLIN SODIUM |
| Strength Number | 10 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
