Package 0363-9812-07

{"route": ["ORAL"], "spl_id": "0c7a4c32-0af5-8e0d-e063-6294a90aebf7", "openfda": {"unii": ["NLJ6390P1Z"], "rxcui": ["2534871"], "spl_set_id": ["bcb81dc1-d854-30c0-e053-2a95a90a9fc7"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (0363-9812-07)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "0363-9812-07", "marketing_start_date": "20211202"}], "brand_name": "Ephedrine Hydrochloride", "product_id": "0363-9812_0c7a4c32-0af5-8e0d-e063-6294a90aebf7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "0363-9812", "generic_name": "Ephedrine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ephedrine Hydrochloride", "active_ingredients": [{"name": "EPHEDRINE HYDROCHLORIDE", "strength": "12.5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211202", "listing_expiration_date": "20261231"}