Package 11673-224-62

Brand: up and up anti diarrheal

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11673-224-62
Digits Only 1167322462
Product NDC 11673-224
Product ID 11673-224_ff50896a-db09-41c2-9b91-55009408ff26
Description

24 BLISTER PACK in 1 CARTON (11673-224-62) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2009-07-20
Brand up and up anti diarrheal
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Up and Up anti diarrheal ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ff50896a-db09-41c2-9b91-55009408ff26", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["ddb70e85-168e-451a-ac04-f6a46721a557"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (11673-224-62)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11673-224-62", "marketing_start_date": "20090720"}], "brand_name": "Up and Up anti diarrheal", "product_id": "11673-224_ff50896a-db09-41c2-9b91-55009408ff26", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "11673-224", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up anti diarrheal", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075232", "marketing_category": "ANDA", "marketing_start_date": "20090720", "listing_expiration_date": "20261231"}