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Levothyroxine Sodium

NDC 60687-453 · American Health Packaging

Generic nameLevothyroxine Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVOTHYROXINE SODIUM
Strength.025 mg/1
Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]
Marketing categoryANDA

Packages

60687-453-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-453-01) / 1 TABLET in 1 BLISTER PACK (60687-453-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 59651-558 — 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, 60687-563 — 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.