Package 68016-204-69

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68016-204-69
Digits Only 6801620469
Product NDC 68016-204
Product ID 68016-204_f73d7997-407d-4a93-99f5-0f2be115cc51
Description

10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68016-204-69)

Marketing

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

Linked Drug Pages (1)

Pseudoephedrine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f73d7997-407d-4a93-99f5-0f2be115cc51", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["aec6412a-b62c-44c8-84f5-77f5fa441028"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68016-204-69)", "package_ndc": "68016-204-69", "marketing_start_date": "20060428"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "68016-204_f73d7997-407d-4a93-99f5-0f2be115cc51", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "68016-204", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "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"}