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LEVOTHYROXINE SODIUM

NDC 68071-3887 · NuCare Pharmaceuticals, Inc.

Generic nameLEVOTHYROXINE SODIUM
Dosage formTABLET
RouteORAL
Active ingredient(s)LEVOTHYROXINE SODIUM
Strength75 ug/1
Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]
Marketing categoryANDA

Packages

68071-3887-3 — 30 TABLET in 1 BOTTLE (68071-3887-3)

68071-3887-9 — 90 TABLET in 1 BOTTLE (68071-3887-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-2048 — Levothyroxine Sodium, 68071-2278 — Levothyroxine Sodium, 68071-2531 — Levothyroxine Sodium, 68071-3619 — Levothyroxine Sodium, 68071-3692 — Levothyroxine Sodium, 68071-3717 — Levothyroxine Sodium, 68071-3730 — Levothyroxine Sodium, 68071-3750 — Levothyroxine Sodium, 68071-3787 — Levothyroxine Sodium, 68071-3814 — Levothyroxine Sodium, 68071-3956 — Levothyroxine Sodium, 68071-3996 — LEVOTHYROXINE SODIUM, 68071-5226 — levothyroxine sodium, 68071-5227 — levothyroxine sodium, 68071-5235 — levothyroxine sodium, 68180-965 — Levothyroxine Sodium, 68180-966 — Levothyroxine Sodium, 68180-967 — Levothyroxine Sodium, 68180-968 — Levothyroxine Sodium, 68180-969 — 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.