Package 50090-5554-0
Brand: pseudoephedrine hydrochloride
Generic: pseudoephedrine hydrochloridePackage Facts
Identity
Package NDC
50090-5554-0
Digits Only
5009055540
Product NDC
50090-5554
Description
10 TABLET, FILM COATED in 1 BLISTER PACK (50090-5554-0)
Marketing
Marketing Status
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": "3b6c8d9e-78df-44be-9bc6-052e19f97706", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["0a2672f0-4e6f-48c9-8571-2d09f06253d7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (50090-5554-0)", "package_ndc": "50090-5554-0", "marketing_start_date": "20210614"}], "brand_name": "Pseudoephedrine hydrochloride", "product_id": "50090-5554_3b6c8d9e-78df-44be-9bc6-052e19f97706", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50090-5554", "generic_name": "Pseudoephedrine hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20271231"}