Package 0904-7409-15

Brand: pseudoephedrine hydrochloride

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-7409-15
Digits Only 0904740915
Product NDC 0904-7409
Product ID 0904-7409_1b23c014-95b2-ac65-e063-6294a90a5d5d
Description

1 BLISTER PACK in 1 CARTON (0904-7409-15) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-06-07
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": "1b23c014-95b2-ac65-e063-6294a90a5d5d", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["658b0fe8-d564-4f79-bbb2-939c518651b7"], "manufacturer_name": ["Major Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0904-7409-15)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7409-15", "marketing_start_date": "20240607"}], "brand_name": "Pseudoephedrine hydrochloride", "product_id": "0904-7409_1b23c014-95b2-ac65-e063-6294a90a5d5d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0904-7409", "generic_name": "Pseudoephedrine hydrochloride", "labeler_name": "Major Pharmaceuticals", "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": "20240607", "listing_expiration_date": "20261231"}