Package 35418-123-12

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 35418-123-12
Digits Only 3541812312
Product NDC 35418-123
Description

2 BLISTER PACK in 1 CARTON (35418-123-12) / 6 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2014-01-16
Brand loperamide hydrochloride
Generic loperamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0ea718d4-6b2b-b9ee-e063-6294a90a8111", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["07e1f89c-5bf6-4539-848a-4435e7deb0d2"], "manufacturer_name": ["Zee Medical Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (35418-123-12)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "35418-123-12", "marketing_start_date": "20140116"}], "brand_name": "Loperamide Hydrochloride", "product_id": "35418-123_0ea718d4-6b2b-b9ee-e063-6294a90a8111", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "35418-123", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Zee Medical Inc", "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": "20140116", "listing_expiration_date": "20261231"}