Glucoheptonate
Glucoheptonate
Approved
Approval ID
ac9f0c4b-d0b0-489a-896d-a92d40f21b7e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 23, 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.
Glucoheptonate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51808-213
Product Classification
G
Generic Name
Glucoheptonate
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 11, 2012
FDA Product Classification
INGREDIENTS (2)
STANNOUS CHLORIDEInactive
Quantity: 0.6 mg in 1 1
Code: 1BQV3749L5
Classification: IACT
CALCIUM GLUCEPTATEActive
Quantity: 50 mg in 1 1
Code: L11651398J
Classification: ACTIB