Package 85766-050-10
Brand: pseudoephedrine hydrochloride
Generic: pseudoephedrine hydrochloridePackage Facts
Identity
Package NDC
85766-050-10
Digits Only
8576605010
Product NDC
85766-050
Description
10 TABLET, FILM COATED in 1 BLISTER PACK (85766-050-10)
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": "4a2c19fc-1529-0713-e063-6394a90a87fe", "openfda": {"unii": ["6V9V2RYJ8N"], "rxcui": ["1049154"], "spl_set_id": ["3b5c81b7-7464-129f-e063-6294a90a48c0"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BLISTER PACK (85766-050-10)", "package_ndc": "85766-050-10", "marketing_start_date": "20250802"}], "brand_name": "Pseudoephedrine hydrochloride", "product_id": "85766-050_4a2c19fc-1529-0713-e063-6394a90a87fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "85766-050", "generic_name": "Pseudoephedrine hydrochloride", "labeler_name": "Sportpharm 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": "20271231"}