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Loperamide hydrochloride - Medication Information

Product NDC Code 70771-1769
Drug Name

Loperamide hydrochloride

Type Generic
Pharm Class Opioid Agonist [EPC],
Opioid Agonists [MoA]
Active Ingredients
Loperamide hydrochloride 2 mg/1
Route ORAL
Dosage Form CAPSULE
RxCUI drug identifier 978006
Application Number ANDA217471
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1769-1 100 capsule in 1 bottle (70771-1769-1)
70771-1769-4 10 blister pack in 1 carton (70771-1769-4) / 10 capsule in 1 blister pack (70771-1769-2)
70771-1769-5 500 capsule in 1 bottle (70771-1769-5)
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Spl product data elements

Usually a list of ingredients in a drug product.
Loperamide hydrochloride Loperamide hydrochloride LOPERAMIDE HYDROCHLORIDE LOPERAMIDE FERRIC OXIDE RED FERRIC OXIDE YELLOW FERROSOFERRIC OXIDE GELATIN LACTOSE MONOHYDRATE MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE 101 MICROCRYSTALLINE CELLULOSE 102 POTASSIUM HYDROXIDE POVIDONE K30 SHELLAC SILICON DIOXIDE SODIUM LAURYL SULFATE SODIUM STARCH GLYCOLATE TYPE A TITANIUM DIOXIDE cream opaque cap cream opaque body 1701

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Loperamide hydrochloride capsules USP, 2 mg NDC 70771-1769-1 100 capsules Rx only 2 mg 100s count

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API