NP Thyroid 60

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 059888437

Effective Date

May 16, 2023

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Levothyroxine(38 ug in 1 1)

Liothyronine(9 ug in 1 1)

Manufacturing Establishments1

FDA-registered manufacturing facilities and establishments involved in the production, packaging, or distribution of this drug product.

Labeler

Asclemed USA, Inc.

DUNS Number

059888437

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

76420-568

Route of Administration

ORAL

Effective Date

May 16, 2023

Ingredients

MINERAL OILInactive

Code: T5L8T28FGPClass: IACT

Code: Q51BO43MG4Class: ACTIBQuantity: 38 ug in 1 1

Code: 06LU7C9H1VClass: ACTIBQuantity: 9 ug in 1 1

CALCIUM STEARATEInactive

Code: 776XM7047LClass: IACT

DEXTROSE MONOHYDRATEInactive

Code: LX22YL083GClass: IACT