NDC 50844-735

Loperamide HCl

Loperamide Hcl

Loperamide HCl is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by L.n.k. International, Inc.. The primary component is Loperamide Hydrochloride.

Product ID50844-735_25c3740b-1fe7-4d26-9df9-98bb7ba97f58
NDC50844-735
Product TypeHuman Otc Drug
Proprietary NameLoperamide HCl
Generic NameLoperamide Hcl
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-05-03
Marketing CategoryANDA / ANDA
Application NumberANDA076497
Labeler NameL.N.K. International, Inc.
Substance NameLOPERAMIDE HYDROCHLORIDE
Active Ingredient Strength2 mg/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 50844-735-02

2 BLISTER PACK in 1 CARTON (50844-735-02) > 6 TABLET in 1 BLISTER PACK
Marketing Start Date2005-05-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50844-735-44 [50844073544]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

NDC 50844-735-08 [50844073508]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

NDC 50844-735-46 [50844073546]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03
Marketing End Date2019-09-24

NDC 50844-735-02 [50844073502]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

NDC 50844-735-24 [50844073524]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

NDC 50844-735-45 [50844073545]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

NDC 50844-735-19 [50844073519]

Loperamide HCl TABLET
Marketing CategoryANDA
Application NumberANDA076497
Product TypeHUMAN OTC DRUG
Marketing Start Date2005-05-03

Drug Details

Active Ingredients

IngredientStrength
LOPERAMIDE HYDROCHLORIDE2 mg/1

OpenFDA Data

SPL SET ID:547c4197-f573-4b30-9e39-2ab11d343609
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 978010

    • NDC Crossover Matching brand name "Loperamide HCl" or generic name "Loperamide Hcl"

    NDCBrand NameGeneric Name
    11673-520Loperamide HClLOPERAMIDE HYDROCHLORIDE
    68016-193Loperamide HClLoperamide HCl
    50844-735Loperamide HClLoperamide HCl
    62011-0158Loperamide HClLoperamide HCl
    10202-2247 Select Anti DiarrhealLoperamide HCl
    10202-6457 select anti diarrhealloperamide HCl
    0113-2224anti diarrhealLoperamide HCl
    0363-1010anti diarrhealLoperamide HCl
    0363-2022Anti Diarrhealloperamide HCl
    0363-0375Anti-DiarrhealLoperamide HCl
    11822-0375Anti-DiarrhealLoperamide HCl
    0498-1071Antidiarrheal ReliefLoperamide HCl
    0113-1645Good Sense antidiarrhealloperamide HCl
    0113-0645good sense loperamide hydrochlorideloperamide HCl
    0113-6004injoy diarrhea reliefLoperamide HCl
    0113-7224loperamide hydrochlorideLoperamide HCl
    0363-0645loperamide hydrochlorideloperamide HCl
    0363-1645loperamide hydrochlorideloperamide HCl
    0904-6256loperamide hydrochlorideloperamide HCl
    0904-6836loperamide hydrochlorideloperamide HCl
    11673-900Up and Up anti diarrhealloperamide HCl
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