Label: CITALOPRAM pellet

  • NDC Code(s): 37662-0336-1, 37662-0336-2, 37662-0336-3, 37662-0337-1, view more
    37662-0337-2, 37662-0337-3, 37662-0338-1, 37662-0338-2, 37662-0338-3, 37662-0338-4, 37662-0339-1, 37662-0339-2, 37662-0339-3, 37662-0339-4, 37662-0340-1, 37662-0340-2, 37662-0340-3, 37662-0340-4, 37662-0341-1, 37662-0341-2, 37662-0341-3, 37662-0341-4, 37662-0342-1, 37662-0342-2, 37662-0342-3, 37662-0342-4, 37662-0343-1
  • Packager: Hahnemann Laboratories, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated June 6, 2022

If you are a consumer or patient please visit this version.

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  • ACTIVE INGREDIENT

  • DOSAGE FORMS & STRENGTHS

  • ACTIVE INGREDIENT

  • PURPOSE

  • INDICATIONS & USAGE

  • WARNINGS

  • PREGNANCY OR BREAST FEEDING

  • ASK DOCTOR

  • KEEP OUT OF REACH OF CHILDREN

  • INSTRUCTIONS FOR USE

  • DOSAGE & ADMINISTRATION

  • ROUTE, METHOD AND FREQUENCY OF ADMINISTRATION

  • INACTIVE INGREDIENT

  • QUESTIONS

  • PRINCIPAL DISPLAY PANEL

    Citalopram 6C 5gCitalopram 6C 30gCitalopram 6C 100gCitalopram 12C 5gCitalopram 12C 30gCitalopram 12C 100gCitalopram 30C 1gCitalopram 30C 5gCitalopram 30C 30gCitalopram 30C 100gCitalopram 100C 1gCitalopram 100C 5gCitalopram 100C 30gCitalopram 100C 100gCitalopram 200C 1gCitalopram 200C 5gCitalopram 200C 30gCitalopram 200C 100gCitalopram 500C 1gCitalopram 500C 5gCitalopram 500C 30gCitalopram 500C 100gCitalopram 1M 1gCitalopram 1M 5gCitalopram 1M 30gCitalopram 1M 100gCitalopram LM1 30g

  • INGREDIENTS AND APPEARANCE
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0339
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM100 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0339-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0339-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0339-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    4NDC:37662-0339-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0343
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM1 [hp_Q]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize1mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0343-110000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0337
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM12 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0337-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0337-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0337-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0336
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM6 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0336-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0336-21200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0336-34000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0338
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM30 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0338-180 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0338-2200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0338-31200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    4NDC:37662-0338-44000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0340
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM200 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0340-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0340-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0340-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    4NDC:37662-0340-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0341
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM500 [hp_C]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0341-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0341-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0341-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    4NDC:37662-0341-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    CITALOPRAM 
    citalopram pellet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37662-0342
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITALOPRAM (UNII: 0DHU5B8D6V) (CITALOPRAM - UNII:0DHU5B8D6V) CITALOPRAM1 [hp_M]
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize2mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37662-0342-1200 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    2NDC:37662-0342-2500 in 1 VIAL, GLASS; Type 0: Not a Combination Product06/06/2022
    3NDC:37662-0342-33000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    4NDC:37662-0342-410000 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic06/06/2022
    Labeler - Hahnemann Laboratories, INC. (147098081)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hahnemann Laboratories, INC.147098081manufacture(37662-0336, 37662-0337, 37662-0338, 37662-0339, 37662-0340, 37662-0341, 37662-0342, 37662-0343)
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