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NDC 67919-0041-05 SIVEXTRO 200 mg/1 Details
SIVEXTRO 200 mg/1
SIVEXTRO is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Merck Sharp & Dohme LLC. The primary component is TEDIZOLID PHOSPHATE.
MedlinePlus Drug Summary
Tedizolid is used to treat skin infections caused by certain types of bacteria in adults and children 12 years of age and older. Tedizolid is in a class of medications called oxazolidinone antibiotics. It works by stopping the growth of bacteria. Antibiotics such as tedizolid will not work for colds, flu, and other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.
Related Packages: 67919-0041-05Last Updated: 04/28/2024
MedLinePlus Full Drug Details: Tedizolid
Product Information
| NDC | 67919-0041 |
|---|---|
| Product ID | 67919-041_282ae0c1-e1f3-4045-af1d-bc2f6bd7b4e2 |
| Associated GPIs | 16230070200320 |
| GCN Sequence Number | 072478 |
| GCN Sequence Number Description | tedizolid phosphate TABLET 200 MG ORAL |
| HIC3 | W1O |
| HIC3 Description | OXAZOLIDINONE ANTIBIOTICS |
| GCN | 36704 |
| HICL Sequence Number | 041209 |
| HICL Sequence Number Description | TEDIZOLID PHOSPHATE |
| Brand/Generic | Brand |
| Proprietary Name | SIVEXTRO |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | tedizolid phosphate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 200 |
| Active Ingredient Units | mg/1 |
| Substance Name | TEDIZOLID PHOSPHATE |
| Labeler Name | Merck Sharp & Dohme LLC |
| Pharmaceutical Class | Breast Cancer Resistance Protein Inhibitors [MoA], Oxazolidinone Antibacterial [EPC], Oxazolidinones [CS] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA205435 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 67919-0041-05 (67919004105)
| NDC Package Code | 67919-041-05 |
|---|---|
| Billing NDC | 67919004105 |
| Package | 1 BLISTER PACK in 1 CARTON (67919-041-05) / 6 TABLET, FILM COATED in 1 BLISTER PACK |
| Marketing Start Date | 2014-06-20 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |