FERROUS SULFATE- ferrous sulfate tablet 
PD-Rx Pharmaceuticals, Inc.

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FERROUS SULFATE
ENTERIC-COATED TABLETS

Dietary Supplement

CONTAINS:

Each tablet contains 324 mg of ferrous sulfate, equivalent to 65 mg of elemental iron, providing 361% of the U.S. recommended daily intake (RDI) of iron for adults and children 4 and older.

DIRECTIONS FOR USE:

Do not crush or chew tablets. Adult Serving Size: 1 tablet two to three times daily. Children: Consult a physician.

WARNING:
Accidental overdose of iron containing products is a leading cause of fatal poisoning in children under 6. Keep this product out of reach of children. In case of accidental overdose, call a doctor or poison control center immediately (1-800-222-1222).

WARNINGS:

Do not take within 2 hours of taking oral tetracycline antibiotics, since oral iron products tend to interfere with absorption of tetracycline. May cause gastrointestinal discomfort, nausea, constipation or diarrhea. If you are pregnant or nursing a baby, seek advice of a health professional before using this product. U.S. Consumer Product Safety Commission requires that iron-containing medicines and vitamins with iron be packaged in child-resistant closures. Parents should always properly resecure safety closures.

STORAGE:

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]

Supplement Facts

Serving Size 1 Tablet
Amount Per Tablet% Daily Value
Iron (from 324 mg of Ferrous Sulfate)65 mg361%

Other ingredients:Microcrystalline Cellulose, Methacrylic Acid Copolymer, Croscarmellose Sodium. Crospovidone, Hypromellose, Stearic Acid, Polydextrose, FD&C Red #40 Lake, Talc, Triacetin, Sodium Lauryl Sulfate, Silicon Dioxide, Triglycerides, Titanium Dioxide, Glycerol Monostearate, Triethyl Citrate, FDC Blue #2 Lake and Polysorbate 80.

16 HOW SUPPLIED

Ferrous Sulfate Tablets are available as follows:

Each tablet contains 324mg of ferrous sulfate, equivalent to 65mg of elemental iron, providing 361% of the U.S. recommended daily intake (RDI) of iron for adults and children 4 and older.

Available in bottles of 100 tablets (72789-436-01)

PRINCIPAL DISPLAY PANEL - 324 mg Tablet Bottle Label

72789-436-01

Ferrous Sulfate
Enteric-Coated
Tablets

324 mg

Dietary
Supplement

Marketed and Packaged By:
PD-Rx Pharmaceuticals, Inc
Oklahoma City, OK 73127
1-405-942-3040 V.12.24.0

100 Tablets
TAMPER EVIDENT: DO NOT USE IF
SAFETY SEAL IS BROKEN OR MISSING FROM BOTTLE.

PRINCIPAL DISPLAY PANEL - 324 mg Tablet Bottle Label
FERROUS SULFATE 
ferrous sulfate tablet
Product Information
Product TypeDIETARY SUPPLEMENTItem Code (Source)NHRIC:72789-436
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FERROUS SULFATE (UNII: 39R4TAN1VT) (FERROUS CATION - UNII:GW89581OWR) FERROUS CATION65 mg
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
METHACRYLIC ACID (UNII: 1CS02G8656)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
CROSPOVIDONE (UNII: 2S7830E561)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
POLYDEXTROSE (UNII: VH2XOU12IE)  
FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T)  
TALC (UNII: 7SEV7J4R1U)  
TRIACETIN (UNII: XHX3C3X673)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
1,2-DILINOLEOYL-3-OLEOYL-SN-GLYCEROL (UNII: 0NXD3O2NER)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
FD&C BLUE NO. 2--ALUMINUM LAKE (UNII: 4AQJ3LG584)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NHRIC:72789-436-01100 in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
DIETARY SUPPLEMENT12/20/2024
Supplement Facts
Serving Size : Serving per Container :
Amount Per Serving% Daily Value
color
scoring1
shape
size (solid drugs)10 mm
Labeler - PD-Rx Pharmaceuticals, Inc. (156893695)
Registrant - PD-Rx Pharmaceuticals, Inc. (156893695)
Establishment
NameAddressID/FEIBusiness Operations
PD-Rx Pharmaceuticals, Inc.156893695repack

Revised: 12/2025
Document Id: b60f6594-b1be-4516-b761-68ebda1ef411
Set id: 7693c763-401d-4665-a984-fbbea72da33e
Version: 10
Effective Time: 20251203
 
PD-Rx Pharmaceuticals, Inc.