linezolid
Generic: linezolid
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
linezolid
Generic Name
linezolid
Labeler
sun pharmaceutical industries, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
linezolid 200 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
57664-682
Product ID
57664-682_2e599906-ac35-54ab-e063-6394a90ac605
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207354
Listing Expiration
2026-12-31
Marketing Start
2017-02-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
57664682
Hyphenated Format
57664-682
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
linezolid (source: ndc)
Generic Name
linezolid (source: ndc)
Application Number
ANDA207354 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/100mL
Packaging
- 100 mL in 1 BAG (57664-682-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2e599906-ac35-54ab-e063-6394a90ac605", "openfda": {"nui": ["N0000175495", "M0361132"], "upc": ["0357664683316", "0357664682302"], "unii": ["ISQ9I6J12J"], "rxcui": ["1662278", "1662285"], "spl_set_id": ["870c9600-04d5-4b44-a5b5-02252a310f22"], "pharm_class_cs": ["Oxazolidinones [CS]"], "pharm_class_epc": ["Oxazolidinone Antibacterial [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BAG (57664-682-30)", "package_ndc": "57664-682-30", "marketing_start_date": "20170201"}], "brand_name": "Linezolid", "product_id": "57664-682_2e599906-ac35-54ab-e063-6394a90ac605", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Oxazolidinone Antibacterial [EPC]", "Oxazolidinones [CS]"], "product_ndc": "57664-682", "generic_name": "linezolid", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Linezolid", "active_ingredients": [{"name": "LINEZOLID", "strength": "200 mg/100mL"}], "application_number": "ANDA207354", "marketing_category": "ANDA", "marketing_start_date": "20170201", "listing_expiration_date": "20261231"}