Skip to main content

Levothyroxine Sodium

NDC 67046-1612 · Coupler LLC

Generic nameLevothyroxine Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVOTHYROXINE SODIUM
Strength125 ug/1
Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]
Marketing categoryNDA AUTHORIZED GENERIC

Packages

67046-1612-3 — 30 TABLET in 1 BLISTER PACK (67046-1612-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-0290 — Levothyroxine Sodium, 67046-0387 — Levothyroxine Sodium, 67046-0515 — Levothyroxine Sodium, 67046-0517 — Levothyroxine Sodium, 67046-0569 — Levothyroxine Sodium, 67046-0801 — Levothyroxine Sodium, 67046-0819 — Levothyroxine Sodium, 67046-0828 — Levothyroxine Sodium, 67046-0951 — Levothyroxine Sodium, 67046-0972 — Levothyroxine Sodium, 67046-1635 — Levothyroxine Sodium, 67046-1679 — LEVOTHYROXINE SODIUM, 67296-1908 — Levothyroxine Sodium, 67296-2046 — Levothyroxine Sodium, 67296-2048 — Levothyroxine Sodium, 68071-2278 — Levothyroxine Sodium, 68071-2531 — Levothyroxine Sodium, 68071-3619 — Levothyroxine Sodium, 68071-3692 — Levothyroxine Sodium, 68071-3717 — 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.