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Claforan
Claforan - 52584-018-01 - (Cefotaxime Sodium)
Drug Information of Claforan
| Product NDC: | 52584-018 |
| Proprietary Name: | Claforan |
| Non Proprietary Name: | Cefotaxime Sodium |
| Active Ingredient(s): | 1 g/g & nbsp; Cefotaxime Sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Claforan
| Product NDC: | 52584-018 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050547 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120607 |
Package Information of Claforan
| Package NDC: | 52584-018-01 |
| Package Description: | 1 VIAL in 1 BAG (52584-018-01) > 1 g in 1 VIAL |
NDC Information of Claforan
| NDC Code | 52584-018-01 |
| Proprietary Name | Claforan |
| Package Description | 1 VIAL in 1 BAG (52584-018-01) > 1 g in 1 VIAL |
| Product NDC | 52584-018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefotaxime Sodium |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20120607 |
| Marketing Category Name | NDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | CEFOTAXIME SODIUM |
| Strength Number | 1 |
| Strength Unit | g/g |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
