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Levothyroxine Sodium

NDC 59651-558 · Aurobindo Pharma Limited

Generic nameLevothyroxine Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVOTHYROXINE SODIUM
Strength300 ug/1
Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]
Marketing categoryANDA

Packages

59651-558-90 — 90 TABLET in 1 BOTTLE (59651-558-90)

59651-558-99 — 1000 TABLET in 1 BOTTLE (59651-558-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-4376 — levothyroxine sodium, 55154-4377 — levothyroxine sodium, 55154-5362 — levothyroxine sodium, 55154-5380 — levothyroxine sodium, 55154-5381 — levothyroxine sodium, 55154-5395 — levothyroxine sodium, 59651-554 — Levothyroxine Sodium, 59651-555 — Levothyroxine Sodium, 59651-556 — Levothyroxine Sodium, 59651-557 — Levothyroxine Sodium, 60687-453 — Levothyroxine Sodium, 60687-464 — Levothyroxine Sodium, 60687-475 — Levothyroxine Sodium, 60687-486 — Levothyroxine Sodium, 60687-497 — Levothyroxine Sodium, 60687-508 — Levothyroxine Sodium, 60687-519 — Levothyroxine Sodium, 60687-530 — Levothyroxine Sodium, 60687-541 — Levothyroxine Sodium, 60687-552 — Levothyroxine Sodium, +547 more

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