Loperamide Hydrochloride

Product NDC
68788-8393
Type
HUMAN OTC DRUG
Nonproprietary name
Loperamide Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206548
Marketing category
ANDA
Substance
LOPERAMIDE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68788-8393-24 BLISTER PACK in 1 CARTON (68788-8393-2) / 6 TABLET in 1 BLISTER PACK20230301NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
5b173bb9-3cca-44ce-9bcb-b9ecc93d3dcfPreferred Pharmaceuticals Inc.2025-07-23HUMAN OTC DRUG LABEL4