Package 58602-715-09

Brand: guaifenesin and dextromethorphan hbr

Generic: guaifenesin and dextromethorphan hbr
NDC Package

Package Facts

Identity

Package NDC 58602-715-09
Digits Only 5860271509
Product NDC 58602-715
Description

1 BOTTLE in 1 CARTON (58602-715-09) / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2017-03-17
Brand guaifenesin and dextromethorphan hbr
Generic guaifenesin and dextromethorphan hbr
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8102c39b-c419-433f-9946-7ef777d7c3ef", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["d0b0ceb8-ef42-4baa-85b3-4d7d2e6f66b7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Aurohealth LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-05)  / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-05", "marketing_start_date": "20170317"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (58602-715-06)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-715-06", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-09)  / 30 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-09", "marketing_start_date": "20170317"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (58602-715-10)  / 8 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-715-10", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-15)  / 60 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-15", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-57)  / 28 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-57", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-60)  / 42 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-60", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (58602-715-64)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-715-64", "marketing_start_date": "20170317"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (58602-715-65)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-715-65", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-68)  / 38 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-68", "marketing_start_date": "20170317"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (58602-715-69)  / 44 TABLET, EXTENDED RELEASE in 1 BOTTLE", "package_ndc": "58602-715-69", "marketing_start_date": "20170317"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (58602-715-70)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "58602-715-70", "marketing_start_date": "20170317"}], "brand_name": "Guaifenesin and Dextromethorphan HBr", "product_id": "58602-715_8102c39b-c419-433f-9946-7ef777d7c3ef", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "58602-715", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "Aurohealth LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan HBr", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA206941", "marketing_category": "ANDA", "marketing_start_date": "20170317", "listing_expiration_date": "20261231"}