NDC 71335-2007 – Levothyroxine sodium

Levothyroxine Sodium 112 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2007

Product details

Brand name
Levothyroxine sodium
Generic name
Levothyroxine Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212399
Marketed since
November 25, 2020
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-2007-130 TABLET in 1 BOTTLE (71335-2007-1)Feb 25, 2022
71335-2007-290 TABLET in 1 BOTTLE (71335-2007-2)Mar 4, 2022
71335-2007-360 TABLET in 1 BOTTLE (71335-2007-3)Dec 11, 2024
71335-2007-418 TABLET in 1 BOTTLE (71335-2007-4)Dec 11, 2024
71335-2007-5100 TABLET in 1 BOTTLE (71335-2007-5)Jul 14, 2023

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