Package 62011-0306-1

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62011-0306-1
Digits Only 6201103061
Product NDC 62011-0306
Description

10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (62011-0306-1)

Marketing

Marketing Status
Marketed Since 2017-02-20
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": "166eaa7e-a180-438e-88b9-6b31bc794b7b", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["918b2a90-532b-4358-bdff-9ad48c167a7e"], "manufacturer_name": ["STRATEGIC SOURCING SERVICES LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (62011-0306-1)", "package_ndc": "62011-0306-1", "marketing_start_date": "20170220"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "62011-0306_166eaa7e-a180-438e-88b9-6b31bc794b7b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "62011-0306", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "STRATEGIC SOURCING SERVICES 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": "20170220", "listing_expiration_date": "20261231"}