Package 53329-664-57

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 53329-664-57
Digits Only 5332966457
Product NDC 53329-664
Product ID 53329-664_2a761ab3-5c74-92c0-e063-6294a90a93aa
Description

12 TABLET in 1 BLISTER PACK (53329-664-57)

Marketing

Marketing Status
Marketed Since 1993-02-01
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": "2a761ab3-5c74-92c0-e063-6294a90a93aa", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["03d68bcf-6413-4fe3-8263-39cc315452d2"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BLISTER PACK (53329-664-57)", "package_ndc": "53329-664-57", "marketing_start_date": "19930201"}], "brand_name": "Loperamide Hydrochloride", "product_id": "53329-664_2a761ab3-5c74-92c0-e063-6294a90a93aa", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "53329-664", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loperamide Hydrochloride", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA074091", "marketing_category": "ANDA", "marketing_start_date": "19930201", "listing_expiration_date": "20261231"}