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NDC 70594-0056-03 Vancomycin 750 mg/150mL Details
Vancomycin 750 mg/150mL
Vancomycin is a INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Xellia Pharmaceuticals USA LLC. The primary component is VANCOMYCIN.
MedlinePlus Drug Summary
Vancomycin injection is used alone or in combination with other medications to treat certain serious infections such as endocarditis (infection of the heart lining and valves), peritonitis (inflammation of the lining of the abdomen), and infections of the lungs, skin, blood, and bones. Vancomycin injection is in a class of medications called glycopeptide antibiotics. It works by killing bacteria that cause infections. Antibiotics such as vancomycin injection will not work for colds, flu, or other viral infections. Taking or using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 70594-0056-03Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Vancomycin Injection
Product Information
| NDC | 70594-0056 |
|---|---|
| Product ID | 70594-056_e49b6589-caca-4c8f-8c57-55a1ee7774cc |
| Associated GPIs | 16280080102053 |
| GCN Sequence Number | 081378 |
| GCN Sequence Number Description | vancomycin/water for inj (PEG) PIGGYBACK 750MG/.15L INTRAVEN |
| HIC3 | W1J |
| HIC3 Description | VANCOMYCIN ANTIBIOTICS AND DERIVATIVES |
| GCN | 48464 |
| HICL Sequence Number | 045612 |
| HICL Sequence Number Description | VANCOMYCIN HCL IN WATER FOR INJECTION (PEG-400, NADA) |
| Brand/Generic | Generic |
| Proprietary Name | Vancomycin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Vancomycin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 750 |
| Active Ingredient Units | mg/150mL |
| Substance Name | VANCOMYCIN |
| Labeler Name | Xellia Pharmaceuticals USA LLC |
| Pharmaceutical Class | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA211962 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70594-0056-03 (70594005603)
| NDC Package Code | 70594-056-03 |
|---|---|
| Billing NDC | 70594005603 |
| Package | 12 BAG in 1 CARTON (70594-056-03) / 150 mL in 1 BAG (70594-056-01) |
| Marketing Start Date | 2020-05-13 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |