NDC 0378-1807 – Levothyroxine Sodium

Levothyroxine Sodium 88 ug/1 · Tablet · Oral

Human Prescription Drug 10 recalls

Product NDC0378-1807

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
November 1, 2002
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
0378-1807-101000 TABLET in 1 BOTTLE, PLASTIC (0378-1807-10)Nov 1, 2002
0378-1807-7790 TABLET in 1 BOTTLE, PLASTIC (0378-1807-77)Jun 27, 2016

Recalls mentioning this NDC

Other Levothyroxine Sodium products