Linezolid

NDC 57664-683 · Sun Pharmaceutical Industries, Inc.

Generic namelinezolid

Dosage formINJECTION, SOLUTION

RouteINTRAVENOUS

Active ingredient(s)LINEZOLID

Strength600 mg/300mL

Pharmacologic classOxazolidinone Antibacterial [EPC], Oxazolidinones [CS]

Marketing categoryANDA

Packages

57664-683-57 — 10 BAG in 1 BOX (57664-683-57) / 300 mL in 1 BAG (57664-683-31)

J2020 — Injection, linezolid, 200 mg Medicare Part B payment limit (ASP + 6%): $2.27

FDA lists these products with the same active ingredient.

0781-3431 — Linezolid, 0781-3433 — Linezolid, 0904-6553 — Linezolid, 31722-749 — Linezolid, 31722-865 — Linezolid, 33342-352 — Linezolid, 43386-022 — Linezolid, 46708-183 — Linezolid, 55150-242 — Linezolid, 57664-682 — linezolid, 59762-1307 — linezolid, 59762-1308 — linezolid, 60687-309 — Linezolid, 60687-754 — Linezolid, 62135-442 — linezolid, 62332-183 — Linezolid, 63323-713 — Linezolid, 63629-8576 — Linezolid, 64980-561 — Linezolid, 65145-181 — 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.