Loperamide Hydrochloride

Product NDC
58602-701
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
58602-701-011 BLISTER PACK in 1 CARTON (58602-701-01) / 6 TABLET in 1 BLISTER PACK2015-12-15NoHistorical
58602-701-022 BLISTER PACK in 1 CARTON (58602-701-02) / 6 TABLET in 1 BLISTER PACK2015-12-15NoHistorical
58602-701-764 BLISTER PACK in 1 CARTON (58602-701-76) / 6 TABLET in 1 BLISTER PACK2015-12-15NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
5b173bb9-3cca-44ce-9bcb-b9ecc93d3dcfPreferred Pharmaceuticals Inc.2025-07-23HUMAN OTC DRUG LABEL4
f3ea8779-252e-4038-ae41-500e15c54825Aurohealth LLC | Aurobindo Pharma Limited2025-01-22Human OTC Drug Label10