Package 69842-973-30
Brand: fexofenadine hydrochloride and pseudoephedrine hydrochloride
Generic: fexofenadine hydrochloride and pseudoephedrine hydrochloridePackage Facts
Identity
Package NDC
69842-973-30
Digits Only
6984297330
Product NDC
69842-973
Description
1 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
Brand
fexofenadine hydrochloride and pseudoephedrine hydrochloride
Generic
fexofenadine hydrochloride and pseudoephedrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "136bd5d9-aea8-4a79-985d-35ddd01de47b", "openfda": {"unii": ["2S068B75ZU", "6V9V2RYJ8N"], "rxcui": ["997406"], "spl_set_id": ["45d3ad69-a80a-4f91-9c9b-8b19a30144a3"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-973-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-973-20", "marketing_start_date": "20200827"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-973-30", "marketing_start_date": "20200827"}], "brand_name": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "product_id": "69842-973_136bd5d9-aea8-4a79-985d-35ddd01de47b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "69842-973", "generic_name": "FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride", "active_ingredients": [{"name": "FEXOFENADINE HYDROCHLORIDE", "strength": "60 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090818", "marketing_category": "ANDA", "marketing_start_date": "20200827", "listing_expiration_date": "20261231"}