NDC 0378-1823 – Levothyroxine Sodium

Levothyroxine Sodium 137 ug/1 · Tablet · Oral

Human Prescription Drug 10 recalls

Product NDC0378-1823

Product details

Brand name
Levothyroxine Sodium
Generic name
levothyroxine sodium
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076187
Marketed since
December 15, 2006
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
0378-1823-101000 TABLET in 1 BOTTLE, PLASTIC (0378-1823-10)Feb 26, 2008
0378-1823-7790 TABLET in 1 BOTTLE, PLASTIC (0378-1823-77)Jun 16, 2016

Recalls mentioning this NDC

Other Levothyroxine Sodium products