Package 43063-801-60
Brand: guaifenesin dm
Generic: guaifenesin and dextromethorphan hydrobromidePackage Facts
Identity
Package NDC
43063-801-60
Digits Only
4306380160
Product NDC
43063-801
Description
60 TABLET in 1 BOTTLE, PLASTIC (43063-801-60)
Marketing
Marketing Status
Brand
guaifenesin dm
Generic
guaifenesin and dextromethorphan hydrobromide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "06c3176d-e6f9-4231-e063-6394a90a694b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0343063801307"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["ac8c0c15-b305-47f2-8712-e4b53636f7fa"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-801-30)", "package_ndc": "43063-801-30", "marketing_end_date": "20271130", "marketing_start_date": "20180402"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-801-60)", "package_ndc": "43063-801-60", "marketing_end_date": "20271130", "marketing_start_date": "20180402"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-801-90)", "package_ndc": "43063-801-90", "marketing_end_date": "20271130", "marketing_start_date": "20180402"}], "brand_name": "Guaifenesin DM", "product_id": "43063-801_06c3176d-e6f9-4231-e063-6394a90a694b", "dosage_form": "TABLET", "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": "43063-801", "generic_name": "GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20271130", "marketing_start_date": "20180402"}