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CEFAZOLIN
CEFAZOLIN - 63323-236-10 - (CEFAZOLIN SODIUM)
Drug Information of CEFAZOLIN
| Product NDC: | 63323-236 |
| Proprietary Name: | CEFAZOLIN |
| Non Proprietary Name: | CEFAZOLIN SODIUM |
| Active Ingredient(s): | 500 mg/2.2mL & nbsp; CEFAZOLIN SODIUM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFAZOLIN
| Product NDC: | 63323-236 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065303 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110715 |
Package Information of CEFAZOLIN
| Package NDC: | 63323-236-10 |
| Package Description: | 25 VIAL in 1 CARTON (63323-236-10) > 2.2 mL in 1 VIAL |
NDC Information of CEFAZOLIN
| NDC Code | 63323-236-10 |
| Proprietary Name | CEFAZOLIN |
| Package Description | 25 VIAL in 1 CARTON (63323-236-10) > 2.2 mL in 1 VIAL |
| Product NDC | 63323-236 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFAZOLIN SODIUM |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20110715 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFAZOLIN SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/2.2mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
