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Levothyroxine Sodium

NDC 60687-541 · American Health Packaging

Generic nameLevothyroxine Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVOTHYROXINE SODIUM
Strength.175 mg/1
Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]
Marketing categoryANDA

Packages

60687-541-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-541-01) / 1 TABLET in 1 BLISTER PACK (60687-541-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-557 — Levothyroxine Sodium, 59651-558 — 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, 60687-552 — Levothyroxine Sodium, 60687-563 — Levothyroxine Sodium, 60793-850 — levothyroxine sodium, 60793-851 — levothyroxine sodium, 60793-852 — levothyroxine sodium, 60793-853 — levothyroxine sodium, 60793-854 — levothyroxine sodium, 60793-855 — levothyroxine sodium, 60793-856 — levothyroxine sodium, 60793-857 — 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.