Product NDC: | 63323-396 |
Proprietary Name: | Cefotetan |
Non Proprietary Name: | CEFOTETAN DISODIUM |
Active Ingredient(s): | 10 g/1 & nbsp; CEFOTETAN DISODIUM |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-396 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065375 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091203 |
Package NDC: | 63323-396-61 |
Package Description: | 1 VIAL in 1 BOX (63323-396-61) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
NDC Code | 63323-396-61 |
Proprietary Name | Cefotetan |
Package Description | 1 VIAL in 1 BOX (63323-396-61) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
Product NDC | 63323-396 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CEFOTETAN DISODIUM |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20091203 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | CEFOTETAN DISODIUM |
Strength Number | 10 |
Strength Unit | g/1 |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |