Package 0904-7472-61

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7472-61
Digits Only 0904747261
Product NDC 0904-7472
Product ID 0904-7472_c42d8eae-ae20-496d-b6a5-d58325ecfc7b
Description

100 BLISTER PACK in 1 CARTON (0904-7472-61) / 1 CAPSULE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-12-20
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": "c42d8eae-ae20-496d-b6a5-d58325ecfc7b", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978006"], "spl_set_id": ["1be585e2-ef49-4210-8a2d-22a326e4cc1b"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7472-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7472-61", "marketing_start_date": "20241220"}], "brand_name": "LOPERAMIDE HYDROCHLORIDE", "product_id": "0904-7472_c42d8eae-ae20-496d-b6a5-d58325ecfc7b", "dosage_form": "CAPSULE", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "0904-7472", "generic_name": "LOPERAMIDE HYDROCHLORIDE", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOPERAMIDE HYDROCHLORIDE", "active_ingredients": [{"name": "LOPERAMIDE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA218122", "marketing_category": "ANDA", "marketing_start_date": "20241220", "listing_expiration_date": "20261231"}