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NP THYROID 90

NP THYROID 90

Approved
Approval ID

dcbb33d6-9bb6-420a-9ee9-4527320d3d5c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 26, 2015

Manufacturers
FDA

Northwind Pharmaceuticals

DUNS: 036986393

Products 1

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

levothyroxine and liothyronine

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code51655-124
Product Classification
G
Generic Name
levothyroxine and liothyronine
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 26, 2015
FDA Product Classification

INGREDIENTS (2)

LEVOTHYROXINEActive
Quantity: 57 ug in 1 1
Code: Q51BO43MG4
Classification: ACTIB
LIOTHYRONINEActive
Quantity: 13.5 ug in 1 1
Code: 06LU7C9H1V
Classification: ACTIB

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NP THYROID 90 - FDA Drug Approval Details