Package 35916-0917-1

{"route": ["ORAL"], "spl_id": "47c778d0-4d3a-074a-e063-6394a90a670c", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1086997"], "spl_set_id": ["37e8ccd5-6be1-9aca-e063-6394a90a5263"], "manufacturer_name": ["SOFTGEL HEALTHCARE PRIVATE LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 POUCH in 1 CARTON (35916-0917-1)  / 3000 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "35916-0917-1", "marketing_start_date": "20250619"}], "brand_name": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "product_id": "35916-0917_47c778d0-4d3a-074a-e063-6394a90a670c", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "35916-0917", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "labeler_name": "SOFTGEL HEALTHCARE PRIVATE LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250619", "listing_expiration_date": "20271231"}