NDC 71335-2562 – Levothyroxine sodium

Levothyroxine Sodium 137 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2562

Product details

Brand name
Levothyroxine sodium
Generic name
Levothyroxine sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207588
Marketed since
September 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 (5)

Package NDCDescriptionSince
71335-2562-130 TABLET in 1 BOTTLE (71335-2562-1)Jan 28, 2025
71335-2562-2100 TABLET in 1 BOTTLE (71335-2562-2)Jan 28, 2025
71335-2562-390 TABLET in 1 BOTTLE (71335-2562-3)Jan 28, 2025
71335-2562-428 TABLET in 1 BOTTLE (71335-2562-4)Jan 28, 2025
71335-2562-560 TABLET in 1 BOTTLE (71335-2562-5)Jan 28, 2025

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