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Levothyroxine Sodium

NDC 68071-3750 · NuCare Pharmaceuticals,Inc.

Generic nameLevothyroxine Sodium

Dosage formTABLET

RouteORAL

Active ingredient(s)LEVOTHYROXINE SODIUM

Strength.05 mg/1

Pharmacologic classThyroxine [CS], l-Thyroxine [EPC]

Marketing categoryANDA

Packages

68071-3750-9 — 90 TABLET in 1 BOTTLE (68071-3750-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68071-3730 — Levothyroxine Sodium, 68071-3787 — Levothyroxine Sodium, 68071-3814 — Levothyroxine Sodium, 68071-3887 — 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, +547 more

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