Package 58602-870-76

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 58602-870-76
Digits Only 5860287076
Product NDC 58602-870
Product ID 58602-870_93ebbb23-a9f0-4519-9793-c9056be39f23
Description

4 BLISTER PACK in 1 CARTON (58602-870-76) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-03-22
Brand loperamide hydrochloride
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Loperamide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "93ebbb23-a9f0-4519-9793-c9056be39f23", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["93ebbb23-a9f0-4519-9793-c9056be39f23"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-870-76)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "58602-870-76", "marketing_start_date": "20220322"}], "brand_name": "Loperamide Hydrochloride", "product_id": "58602-870_93ebbb23-a9f0-4519-9793-c9056be39f23", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "58602-870", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA206548", "marketing_category": "ANDA", "marketing_start_date": "20220322", "listing_expiration_date": "20261231"}