Package 21130-204-21

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 21130-204-21
Digits Only 2113020421
Product NDC 21130-204
Description

20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-204-21)

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": "22744b1f-71f8-4db8-b2d5-1da1ea2a452a", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["01a5d9dd-f123-443b-b968-412c0aadaaa2"], "manufacturer_name": ["Safeway Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-204-21)", "package_ndc": "21130-204-21", "marketing_start_date": "20060428"}, {"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (21130-204-69)", "package_ndc": "21130-204-69", "marketing_start_date": "20060428"}], "brand_name": "Pseudoephedrine Hydrochloride", "product_id": "21130-204_22744b1f-71f8-4db8-b2d5-1da1ea2a452a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "21130-204", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Safeway 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"}