Loperamide Hydrochloride

Product NDC
58602-870
Type
HUMAN OTC DRUG
Nonproprietary name
Loperamide Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Aurohealth LLC
Application
ANDA206548
Marketing category
ANDA
Substance
LOPERAMIDE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
58602-870-764 BLISTER PACK in 1 CARTON (58602-870-76) / 6 TABLET in 1 BLISTER PACK2022-03-22NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
93ebbb23-a9f0-4519-9793-c9056be39f23Aurohealth LLC | Aurobindo Pharma Limited2022-03-22Human OTC Drug Label1