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CEFTRIAXONE
CEFTRIAXONE - 55648-701-02 - (CEFTRIAXONE)
Drug Information of CEFTRIAXONE
| Product NDC: | 55648-701 |
| Proprietary Name: | CEFTRIAXONE |
| Non Proprietary Name: | CEFTRIAXONE |
| Active Ingredient(s): | 250 mg/1 & nbsp; CEFTRIAXONE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFTRIAXONE
| Product NDC: | 55648-701 |
| Labeler Name: | Wockhardt Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065391 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070412 |
Package Information of CEFTRIAXONE
| Package NDC: | 55648-701-02 |
| Package Description: | 10 INJECTION, POWDER, FOR SOLUTION in 1 BOX (55648-701-02) |
NDC Information of CEFTRIAXONE
| NDC Code | 55648-701-02 |
| Proprietary Name | CEFTRIAXONE |
| Package Description | 10 INJECTION, POWDER, FOR SOLUTION in 1 BOX (55648-701-02) |
| Product NDC | 55648-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFTRIAXONE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20070412 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt Limited |
| Substance Name | CEFTRIAXONE SODIUM |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
