NDC 71335-2549 – Levothyroxine Sodium

Levothyroxine Sodium .025 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2549

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209713
Marketed since
March 20, 2019
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-2549-130 TABLET in 1 BOTTLE (71335-2549-1)Jan 21, 2025
71335-2549-290 TABLET in 1 BOTTLE (71335-2549-2)Jan 21, 2025
71335-2549-3100 TABLET in 1 BOTTLE (71335-2549-3)Jan 21, 2025
71335-2549-460 TABLET in 1 BOTTLE (71335-2549-4)Jan 21, 2025
71335-2549-528 TABLET in 1 BOTTLE (71335-2549-5)Jan 21, 2025
71335-2549-610 TABLET in 1 BOTTLE (71335-2549-6)Jan 21, 2025

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