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Cefotetan
Cefotetan - 63323-385-10 - (CEFOTETAN DISODIUM)
Drug Information of Cefotetan
| Product NDC: | 63323-385 |
| Proprietary Name: | Cefotetan |
| Non Proprietary Name: | CEFOTETAN DISODIUM |
| Active Ingredient(s): | 1 g/10mL & nbsp; CEFOTETAN DISODIUM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefotetan
| Product NDC: | 63323-385 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065374 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091118 |
Package Information of Cefotetan
| Package NDC: | 63323-385-10 |
| Package Description: | 10 VIAL in 1 TRAY (63323-385-10) > 10 mL in 1 VIAL |
NDC Information of Cefotetan
| NDC Code | 63323-385-10 |
| Proprietary Name | Cefotetan |
| Package Description | 10 VIAL in 1 TRAY (63323-385-10) > 10 mL in 1 VIAL |
| Product NDC | 63323-385 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFOTETAN DISODIUM |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20091118 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFOTETAN DISODIUM |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
