NDC 69238-1839 – Levothyroxine Sodium

Levothyroxine Sodium .175 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69238-1839

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021210
Marketed since
December 1, 2003
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
69238-1839-1100 TABLET in 1 BOTTLE, PLASTIC (69238-1839-1)Dec 1, 2003
69238-1839-71000 TABLET in 1 BOTTLE, PLASTIC (69238-1839-7)Dec 1, 2003

Other Levothyroxine Sodium products