Armour Thyroid
Armour Thyroid (thyroid tablets, USP)
Approved
Approval ID
82cc78b5-20f2-4a4d-a633-012ed0542c09
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 26, 2023
Manufacturers
FDA
PD-Rx Pharmaceuticals, Inc.
DUNS: 156893695
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
THYROID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code43063-345
Product Classification
G
Generic Name
THYROID
Product Specifications
Route of AdministrationORAL
Effective DateSeptember 26, 2023
FDA Product Classification
INGREDIENTS (5)
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
DEXTROSEInactive
Code: IY9XDZ35W2
Classification: IACT
CALCIUM STEARATEInactive
Code: 776XM7047L
Classification: IACT
SUS SCROFA THYROIDActive
Quantity: 30 mg in 1 1
Code: 6RV024OAUQ
Classification: ACTIB