Package 63868-143-10

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63868-143-10
Digits Only 6386814310
Product NDC 63868-143
Description

10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10)

Marketing

Marketing Status
Marketed Since 2006-04-28
Brand pseudoephedrine hydrochloride
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4cc7999a-1c1f-49a9-af68-4ad045f3496a", "openfda": {"upc": ["0635515957855"], "unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["880d368f-0ce3-4993-b5b1-13bf01310516"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (63868-143-10)", "package_ndc": "63868-143-10", "marketing_start_date": "20060428"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "63868-143_4cc7999a-1c1f-49a9-af68-4ad045f3496a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "63868-143", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA077442", "marketing_category": "ANDA", "marketing_start_date": "20060428", "listing_expiration_date": "20261231"}