ARMOUR THYROID
Armour® Thyroid (thyroid tablets, USP)
Approved
Approval ID
7617f4a4-8812-44c4-8386-bc991f4d3a77
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 27, 2011
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 2
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 Code42254-104
Product Classification
G
Generic Name
THYROID
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2010
FDA Product Classification
INGREDIENTS (5)
CALCIUM STEARATEInactive
Code: 776XM7047L
Classification: IACT
POWDERED CELLULOSEInactive
Code: SMD1X3XO9M
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
DEXTROSEInactive
Code: IY9XDZ35W2
Classification: IACT
THYROIDActive
Quantity: 15 mg in 1 1
Code: 0B4FDL9I6P
Classification: ACTIB
THYROID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code42254-105
Product Classification
G
Generic Name
THYROID
Product Specifications
Route of AdministrationORAL
Effective DateOctober 27, 2010
FDA Product Classification
INGREDIENTS (5)
POWDERED CELLULOSEInactive
Code: SMD1X3XO9M
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
CALCIUM STEARATEInactive
Code: 776XM7047L
Classification: IACT
DEXTROSEInactive
Code: IY9XDZ35W2
Classification: IACT
THYROIDActive
Quantity: 30 mg in 1 1
Code: 0B4FDL9I6P
Classification: ACTIB