NDC 67877-419 – Linezolid

Linezolid 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67877-419

Product details

Brand name
Linezolid
Generic name
Linezolid
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205517
Marketed since
December 21, 2015
Listing expires
December 31, 2026
Pharmacologic class
Oxazolidinone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Linezolid →

Package NDC codes (8)

Package NDCDescriptionSince
67877-419-01100 TABLET, FILM COATED in 1 BOTTLE (67877-419-01)Dec 21, 2015
67877-419-05500 TABLET, FILM COATED in 1 BOTTLE (67877-419-05)Dec 21, 2015
67877-419-101000 TABLET, FILM COATED in 1 BOTTLE (67877-419-10)Dec 21, 2015
67877-419-2020 TABLET, FILM COATED in 1 BOTTLE (67877-419-20)Dec 21, 2015
67877-419-331 BLISTER PACK in 1 CARTON (67877-419-33) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 21, 2015
67877-419-3810 BLISTER PACK in 1 CARTON (67877-419-38) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 21, 2015
67877-419-843 BLISTER PACK in 1 CARTON (67877-419-84) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 21, 2015
67877-419-852 BLISTER PACK in 1 CARTON (67877-419-85) / 10 TABLET, FILM COATED in 1 BLISTER PACKDec 21, 2015

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