Package 63304-106-21
Brand: guaifenesin and dextromethorphan hbr
Generic: guaifenesin and dextromethorphan hbrPackage Facts
Identity
Package NDC
63304-106-21
Digits Only
6330410621
Product NDC
63304-106
Description
1 BLISTER PACK in 1 CARTON (63304-106-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Marketing
Marketing Status
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": "801949ca-1baf-4a19-8466-91b4269a2c63", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074", "1298324"], "spl_set_id": ["06328741-03e3-49cf-ae44-d4c2116e38a3"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["SUN PHARMACEUTICAL INDUSTRIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63304-106-21) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63304-106-21", "marketing_start_date": "20210701"}], "brand_name": "Guaifenesin and Dextromethorphan HBr", "product_id": "63304-106_801949ca-1baf-4a19-8466-91b4269a2c63", "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": "63304-106", "generic_name": "Guaifenesin and Dextromethorphan HBr", "labeler_name": "SUN PHARMACEUTICAL INDUSTRIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan HBr", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}, {"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA214781", "marketing_category": "ANDA", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}