NDC 42292-038 – Levothyroxine Sodium

Levothyroxine Sodium 88 ug/1 · Tablet · Oral

Human Prescription Drug 3 recalls

Product NDC42292-038

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine sodium
Labeler
Mylan Institutional Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076187
Marketed since
January 18, 2017
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
42292-038-20100 BLISTER PACK in 1 CARTON (42292-038-20) / 1 TABLET in 1 BLISTER PACK (42292-038-01)Jan 18, 2017

Recalls mentioning this NDC

Other Levothyroxine Sodium products