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CEFTRIAXONE
CEFTRIAXONE - 49349-835-41 - (CEFTRIAXONE)
Drug Information of CEFTRIAXONE
| Product NDC: | 49349-835 |
| Proprietary Name: | CEFTRIAXONE |
| Non Proprietary Name: | CEFTRIAXONE |
| Active Ingredient(s): | 1 g/1 & nbsp; CEFTRIAXONE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFTRIAXONE
| Product NDC: | 49349-835 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065180 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130613 |
Package Information of CEFTRIAXONE
| Package NDC: | 49349-835-41 |
| Package Description: | 10 INJECTION, POWDER, FOR SOLUTION in 1 BOX (49349-835-41) |
NDC Information of CEFTRIAXONE
| NDC Code | 49349-835-41 |
| Proprietary Name | CEFTRIAXONE |
| Package Description | 10 INJECTION, POWDER, FOR SOLUTION in 1 BOX (49349-835-41) |
| Product NDC | 49349-835 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFTRIAXONE |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20130613 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CEFTRIAXONE SODIUM |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
