Linezolid

NDC 31722-749 · Camber Pharmaceuticals, Inc.

Generic nameLinezolid

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LINEZOLID

Strength600 mg/1

Pharmacologic classOxazolidinone Antibacterial [EPC], Oxazolidinones [CS]

Marketing categoryANDA

Packages

31722-749-01 — 100 TABLET, FILM COATED in 1 BOTTLE (31722-749-01)

31722-749-20 — 20 TABLET, FILM COATED in 1 BOTTLE (31722-749-20)

31722-749-30 — 30 TABLET, FILM COATED in 1 BOTTLE (31722-749-30)

31722-749-31 — 150 TABLET, FILM COATED in 1 CARTON (31722-749-31)

FDA lists these products with the same active ingredient.

0009-5136 — linezolid, 0009-5138 — linezolid, 0009-5140 — linezolid, 0009-7807 — linezolid, 0054-0319 — linezolid, 0143-9534 — Linezolid, 0409-4883 — LINEZOLID, 0781-3431 — Linezolid, 0781-3433 — Linezolid, 0904-6553 — Linezolid, 31722-865 — Linezolid, 33342-352 — Linezolid, 43386-022 — Linezolid, 46708-183 — Linezolid, 55150-242 — Linezolid, 57664-682 — linezolid, 57664-683 — linezolid, 59762-1307 — linezolid, 59762-1308 — linezolid, 60687-309 — Linezolid, +19 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.