Package 55315-123-06

Brand: loperamide hydrochloride

Generic: loperamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55315-123-06
Digits Only 5531512306
Product NDC 55315-123
Description

6 TABLET in 1 BLISTER PACK (55315-123-06)

Marketing

Marketing Status
Marketed Since 1993-02-01
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": "0ea71b09-2bcf-8966-e063-6294a90a813e", "openfda": {"unii": ["77TI35393C"], "rxcui": ["978010"], "spl_set_id": ["a3bf91ae-22f3-4402-b73c-de026f2d0475"], "manufacturer_name": ["Fred's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET in 1 BLISTER PACK (55315-123-06)", "package_ndc": "55315-123-06", "marketing_start_date": "19930201"}, {"sample": false, "description": "24 TABLET in 1 BLISTER PACK (55315-123-24)", "package_ndc": "55315-123-24", "marketing_start_date": "19930201"}], "brand_name": "Loperamide Hydrochloride", "product_id": "55315-123_0ea71b09-2bcf-8966-e063-6294a90a813e", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "55315-123", "generic_name": "Loperamide Hydrochloride", "labeler_name": "Fred's 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": "19930201", "listing_expiration_date": "20261231"}