NDC 68071-3887 – Levothyroxine Sodium

Levothyroxine Sodium 75 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3887

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211417
Marketed since
April 8, 2025
Listing expires
December 31, 2027
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
68071-3887-330 TABLET in 1 BOTTLE (68071-3887-3)Jan 7, 2026
68071-3887-990 TABLET in 1 BOTTLE (68071-3887-9)Aug 28, 2025

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