Skip to main content

Levothyroxine Sodium

NDC 68180-965 · Lupin Pharmaceuticals, Inc.

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

Packages

68180-965-01 — 100 TABLET in 1 BOTTLE (68180-965-01)

68180-965-03 — 1000 TABLET in 1 BOTTLE (68180-965-03)

68180-965-09 — 90 TABLET in 1 BOTTLE (68180-965-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3730 — Levothyroxine Sodium, 68071-3750 — 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, 68180-966 — Levothyroxine Sodium, 68180-967 — Levothyroxine Sodium, 68180-968 — Levothyroxine Sodium, 68180-969 — Levothyroxine Sodium, 68180-970 — Levothyroxine Sodium, 68180-971 — Levothyroxine Sodium, 68180-972 — Levothyroxine Sodium, 68180-973 — Levothyroxine Sodium, 68180-974 — Levothyroxine Sodium, 68180-975 — 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.