linezolid

Generic: linezolid

Labeler: ascend laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name linezolid
Generic Name linezolid
Labeler ascend laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

linezolid 600 mg/1

Manufacturer
Ascend Laboratories, LLC

Identifiers & Regulatory

Product NDC 67877-419
Product ID 67877-419_1dd1fb9c-98f4-4e25-8246-fb8462ff381c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205517
Listing Expiration 2026-12-31
Marketing Start 2015-12-21

Pharmacologic Class

Established (EPC)
oxazolidinone antibacterial [epc]
Chemical Structure
oxazolidinones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67877419
Hyphenated Format 67877-419

Supplemental Identifiers

RxCUI
311347
UNII
ISQ9I6J12J
NUI
N0000175495 M0361132

Packaging Origin

Original Packager
true

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 ANDA205517 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (67877-419-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (67877-419-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (67877-419-10)
  • 20 TABLET, FILM COATED in 1 BOTTLE (67877-419-20)
  • 1 BLISTER PACK in 1 CARTON (67877-419-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 10 BLISTER PACK in 1 CARTON (67877-419-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (67877-419-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (67877-419-85) / 10 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (8)

67877-419-01 100 TABLET, FILM COATED in 1 BOTTLE (67877-419-01) 67877-419-05 500 TABLET, FILM COATED in 1 BOTTLE (67877-419-05) 67877-419-10 1000 TABLET, FILM COATED in 1 BOTTLE (67877-419-10) 67877-419-20 20 TABLET, FILM COATED in 1 BOTTLE (67877-419-20) 67877-419-33 1 BLISTER PACK in 1 CARTON (67877-419-33) / 10 TABLET, FILM COATED in 1 BLISTER PACK 67877-419-38 10 BLISTER PACK in 1 CARTON (67877-419-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK 67877-419-84 3 BLISTER PACK in 1 CARTON (67877-419-84) / 10 TABLET, FILM COATED in 1 BLISTER PACK 67877-419-85 2 BLISTER PACK in 1 CARTON (67877-419-85) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

linezolid (600 mg/1)

Linked Drug Pages (1)

Linezolid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1dd1fb9c-98f4-4e25-8246-fb8462ff381c", "openfda": {"nui": ["N0000175495", "M0361132"], "unii": ["ISQ9I6J12J"], "rxcui": ["311347"], "spl_set_id": ["7402aa01-50de-46c8-a341-d30da5b32b1c"], "pharm_class_cs": ["Oxazolidinones [CS]"], "pharm_class_epc": ["Oxazolidinone Antibacterial [EPC]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (67877-419-01)", "package_ndc": "67877-419-01", "marketing_start_date": "20151221"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-419-05)", "package_ndc": "67877-419-05", "marketing_start_date": "20151221"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (67877-419-10)", "package_ndc": "67877-419-10", "marketing_start_date": "20151221"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (67877-419-20)", "package_ndc": "67877-419-20", "marketing_start_date": "20151221"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67877-419-33)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-419-33", "marketing_start_date": "20151221"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-419-38)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-419-38", "marketing_start_date": "20151221"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (67877-419-84)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-419-84", "marketing_start_date": "20151221"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (67877-419-85)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-419-85", "marketing_start_date": "20151221"}], "brand_name": "Linezolid", "product_id": "67877-419_1dd1fb9c-98f4-4e25-8246-fb8462ff381c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Oxazolidinone Antibacterial [EPC]", "Oxazolidinones [CS]"], "product_ndc": "67877-419", "generic_name": "Linezolid", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Linezolid", "active_ingredients": [{"name": "LINEZOLID", "strength": "600 mg/1"}], "application_number": "ANDA205517", "marketing_category": "ANDA", "marketing_start_date": "20151221", "listing_expiration_date": "20261231"}