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Rocephin
Rocephin - 0004-1963-01 - (ceftriaxone sodium)
Drug Information of Rocephin
| Product NDC: | 0004-1963 |
| Proprietary Name: | Rocephin |
| Non Proprietary Name: | ceftriaxone sodium |
| Active Ingredient(s): | 500 mg/1 & nbsp; ceftriaxone sodium |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rocephin
| Product NDC: | 0004-1963 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063239 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930813 |
Package Information of Rocephin
| Package NDC: | 0004-1963-01 |
| Package Description: | 10 VIAL, GLASS in 1 BOX (0004-1963-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS |
NDC Information of Rocephin
| NDC Code | 0004-1963-01 |
| Proprietary Name | Rocephin |
| Package Description | 10 VIAL, GLASS in 1 BOX (0004-1963-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS |
| Product NDC | 0004-1963 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ceftriaxone sodium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 19930813 |
| Marketing Category Name | ANDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | CEFTRIAXONE SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
