Integra F
see all prescribing information for Integra F
Approved
Approval ID
025fee85-53a8-4161-a806-44fd95d0ca74
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 8, 2022
Manufacturers
FDA
U.S. Pharmaceutical Corporation
DUNS: 079467662
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52747-711
Product Classification
G
Generic Name
Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid
Product Specifications
Route of AdministrationORAL
Effective DateJuly 13, 2022
FDA Product Classification
INGREDIENTS (10)
FERROUS FUMARATEActive
Quantity: 62.5 mg in 1 1
Code: R5L488RY0Q
Classification: ACTIM
ASCORBIC ACIDActive
Quantity: 40 mg in 1 1
Code: PQ6CK8PD0R
Classification: ACTIB
NIACINActive
Quantity: 3 mg in 1 1
Code: 2679MF687A
Classification: ACTIB
FERROUS ASPARTO GLYCINATEActive
Quantity: 62.5 mg in 1 1
Code: H7426RGB3L
Classification: ACTIM
FOLIC ACIDActive
Quantity: 1 mg in 1 1
Code: 935E97BOY8
Classification: ACTIB
HYPROMELLOSE, UNSPECIFIEDInactive
Code: 3NXW29V3WO
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT