Package 0280-0506-20

{"route": ["ORAL"], "spl_id": "45266d30-bb3b-21f8-e063-6294a90a29cf", "openfda": {"upc": ["0016500559542"], "rxcui": ["1297288", "1432488", "1927849"], "spl_set_id": ["5278a128-41ec-4494-e054-00144ff8d46c"], "manufacturer_name": ["Bayer HealthCare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0280-0506-20)  *  2 BLISTER PACK in 1 CARTON / 6 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  2 BLISTER PACK in 1 CARTON / 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "0280-0506-20", "marketing_start_date": "20170530"}], "brand_name": "Alka-Seltzer Plus Severe Cough Mucus and Congestion Day and Night", "product_id": "0280-0506_45266d30-bb3b-21f8-e063-6294a90a29cf", "dosage_form": "KIT", "product_ndc": "0280-0506", "generic_name": "Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride, Guaifenesin", "labeler_name": "Bayer HealthCare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Alka-Seltzer Plus Severe Cough Mucus and Congestion Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}