Product NDC: | 52584-023 |
Proprietary Name: | Cefazolin |
Non Proprietary Name: | Cefazolin Sodium |
Active Ingredient(s): | 1 g/3mL & nbsp; Cefazolin Sodium |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-023 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065226 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110907 |
Package NDC: | 52584-023-10 |
Package Description: | 1 VIAL in 1 BAG (52584-023-10) > 3 mL in 1 VIAL |
NDC Code | 52584-023-10 |
Proprietary Name | Cefazolin |
Package Description | 1 VIAL in 1 BAG (52584-023-10) > 3 mL in 1 VIAL |
Product NDC | 52584-023 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cefazolin Sodium |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110907 |
Marketing Category Name | ANDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | CEFAZOLIN SODIUM |
Strength Number | 1 |
Strength Unit | g/3mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |