Package 67296-1472-7

Brand: anti diarrheal

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-1472-7
Digits Only 6729614727
Product NDC 67296-1472
Description

24 TABLET, FILM COATED in 1 BOTTLE (67296-1472-7)

Marketing

Marketing Status
Marketed Since 2003-02-24
Brand anti diarrheal
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c62c754-9698-47f7-e063-6294a90a94fe", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["f4c23673-056e-7608-e053-2995a90a9276"], "manufacturer_name": ["Redpharm Drug Inc"]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (67296-1472-7)", "package_ndc": "67296-1472-7", "marketing_start_date": "20030224"}], "brand_name": "anti diarrheal", "product_id": "67296-1472_2c62c754-9698-47f7-e063-6294a90a94fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "67296-1472", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Redpharm Drug Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "anti diarrheal", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA075232", "marketing_category": "ANDA", "marketing_start_date": "20030224", "listing_expiration_date": "20261231"}