Package 71335-9616-1
Brand: guaifenesin
Generic: guaifenesinPackage Facts
Identity
Package NDC
71335-9616-1
Digits Only
7133596161
Product NDC
71335-9616
Description
30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)
Marketing
Marketing Status
Brand
guaifenesin
Generic
guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "97d545be-a78d-48b5-b774-ded0e82d742f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["570a71eb-2d19-4c7b-8c00-e1524bfa3844"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71335-9616-1)", "package_ndc": "71335-9616-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (71335-9616-2)", "package_ndc": "71335-9616-2", "marketing_start_date": "20221228"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (71335-9616-3)", "package_ndc": "71335-9616-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71335-9616-4)", "package_ndc": "71335-9616-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE, PLASTIC (71335-9616-5)", "package_ndc": "71335-9616-5", "marketing_start_date": "20240403"}], "brand_name": "Guaifenesin", "product_id": "71335-9616_97d545be-a78d-48b5-b774-ded0e82d742f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "71335-9616", "generic_name": "Guaifenesin", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}