Thyrotropin Releasing Hormone
Thyrotropin-Releasing Hormone
Approved
Approval ID
af5da799-76bf-415a-9dc7-99c7ddc62bc4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 19, 2012
Manufacturers
FDA
AnazaoHealth Corporation
DUNS: 011038762
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Thyrotropin Releasing Hormone
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51808-209
Product Classification
G
Generic Name
Thyrotropin Releasing Hormone
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 15, 2012
FDA Product Classification
INGREDIENTS (4)
PROPYLPARABENInactive
Quantity: 0.2 mg in 1 mL
Code: Z8IX2SC1OH
Classification: IACT
METHYLPARABENInactive
Quantity: 1.8 mg in 1 mL
Code: A2I8C7HI9T
Classification: IACT
PROTIRELINActive
Quantity: 500 ug in 1 mL
Code: 5Y5F15120W
Classification: ACTIB
SODIUM CHLORIDEInactive
Quantity: 9 mg in 1 mL
Code: 451W47IQ8X
Classification: IACT