NDC 51079-445 – Levothyroxine Sodium

Levothyroxine Sodium 150 ug/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC51079-445

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
February 26, 2007
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
51079-445-20100 BLISTER PACK in 1 CARTON (51079-445-20) / 1 TABLET in 1 BLISTER PACK (51079-445-01)Feb 26, 2007

Recalls mentioning this NDC

Other Levothyroxine Sodium products