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Ceftriaxone
Ceftriaxone - 55390-316-01 - (Ceftriaxone)
Drug Information of Ceftriaxone
| Product NDC: | 55390-316 |
| Proprietary Name: | Ceftriaxone |
| Non Proprietary Name: | Ceftriaxone |
| Active Ingredient(s): | 100 mg/mL & nbsp; Ceftriaxone |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ceftriaxone
| Product NDC: | 55390-316 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065475 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090722 |
Package Information of Ceftriaxone
| Package NDC: | 55390-316-01 |
| Package Description: | 1 VIAL, PHARMACY BULK PACKAGE in 1 BOX, UNIT-DOSE (55390-316-01) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Ceftriaxone
| NDC Code | 55390-316-01 |
| Proprietary Name | Ceftriaxone |
| Package Description | 1 VIAL, PHARMACY BULK PACKAGE in 1 BOX, UNIT-DOSE (55390-316-01) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 55390-316 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ceftriaxone |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090722 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | CEFTRIAXONE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
