NDC 0074-7068 – Synthroid

Levothyroxine Sodium 125 ug/1 · Tablet · Oral

Human Prescription Drug 5 recalls

Product NDC0074-7068

Product details

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

Active ingredients

Uses, dosage, side effects and warnings for Synthroid →

Package NDC codes (4)

Package NDCDescriptionSince
0074-7068-1110 BLISTER PACK in 1 BOX, UNIT-DOSE (0074-7068-11) / 10 TABLET in 1 BLISTER PACKJul 24, 2002
0074-7068-191000 TABLET in 1 BOTTLE (0074-7068-19)Jul 24, 2002
0074-7068-72 sample2 BLISTER PACK in 1 CARTON (0074-7068-72) / 7 TABLET in 1 BLISTER PACKJul 24, 2002
0074-7068-9090 TABLET in 1 BOTTLE (0074-7068-90)Jul 24, 2002

Recalls mentioning this NDC

Other Synthroid products