Package 69367-415-01

{"route": ["ORAL"], "spl_id": "46766222-63b4-478f-aa8b-a23b20476317", "openfda": {"nui": ["N0000175790", "M0023046"], "upc": ["0369367414012", "0369367415019"], "unii": ["0I55128JYK"], "rxcui": ["313291", "348472"], "spl_set_id": ["04f1d1da-ce61-45b3-acf4-903cc81d16da"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-415-01)", "package_ndc": "69367-415-01", "marketing_start_date": "20251125"}], "brand_name": "Theophylline (Anhydrous)", "product_id": "69367-415_46766222-63b4-478f-aa8b-a23b20476317", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "69367-415", "generic_name": "Theophylline Anhydrous", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "brand_name_suffix": "(Anhydrous)", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "600 mg/1"}], "application_number": "ANDA040560", "marketing_category": "ANDA", "marketing_start_date": "20251125", "listing_expiration_date": "20261231"}