NDC 33342-395 – Levothyroxine Sodium

Levothyroxine Sodium 75 ug/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC33342-395

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211417
Marketed since
December 21, 2022
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

Uses, dosage, side effects and warnings for Levothyroxine Sodium →

Package NDC codes (3)

Package NDCDescriptionSince
33342-395-1090 TABLET in 1 BOTTLE (33342-395-10)Dec 21, 2022
33342-395-11100 TABLET in 1 BOTTLE (33342-395-11)Dec 21, 2022
33342-395-441000 TABLET in 1 BOTTLE (33342-395-44)Jan 24, 2023

Recalls mentioning this NDC

Other Levothyroxine Sodium products