NDC 0074-7148 – Synthroid

Levothyroxine Sodium 200 ug/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC0074-7148

Product details

Brand name
Synthroid
Generic name
Levothyroxine Sodium
Labeler
AbbVie Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA021402
Marketed since
February 24, 2002
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

Uses, dosage, side effects and warnings for Synthroid →

Package NDC codes (3)

Package NDCDescriptionSince
0074-7148-1110 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-7148-11) / 10 TABLET in 1 BLISTER PACKFeb 24, 2002
0074-7148-191000 TABLET in 1 BOTTLE (0074-7148-19)Feb 24, 2002
0074-7148-9090 TABLET in 1 BOTTLE (0074-7148-90)Feb 24, 2002

Recalls mentioning this NDC

Other Synthroid products