NDC 68180-966 – Levothyroxine Sodium

Levothyroxine Sodium .05 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68180-966

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209713
Marketed since
May 2, 2019
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68180-966-01100 TABLET in 1 BOTTLE (68180-966-01)May 2, 2019
68180-966-031000 TABLET in 1 BOTTLE (68180-966-03)May 2, 2019
68180-966-0990 TABLET in 1 BOTTLE (68180-966-09)May 2, 2019

Recalls mentioning this NDC

Other Levothyroxine Sodium products