Package 85766-048-10
Brand: loratadine and pseudoephedrine
Generic: loratadine and pseudoephedrinePackage Facts
Identity
Package NDC
85766-048-10
Digits Only
8576604810
Product NDC
85766-048
Description
1 BLISTER PACK in 1 CARTON (85766-048-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
Brand
loratadine and pseudoephedrine
Generic
loratadine and pseudoephedrine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4a2c2629-df77-dec0-e063-6394a90a45a4", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["2b432b67-f9f3-45e2-8306-2d4080152f99"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (85766-048-10) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "85766-048-10", "marketing_start_date": "20250802"}], "brand_name": "Loratadine and Pseudoephedrine", "product_id": "85766-048_4a2c2629-df77-dec0-e063-6394a90a45a4", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "85766-048", "generic_name": "loratadine and pseudoephedrine", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20041117", "listing_expiration_date": "20271231"}