Package 17714-152-01

Brand: mucus relief

Generic: guaifenesin 400 mg
NDC Package

Package Facts

Identity

Package NDC 17714-152-01
Digits Only 1771415201
Product NDC 17714-152
Description

100 TABLET in 1 BOTTLE (17714-152-01)

Marketing

Marketing Status
Marketed Since 2016-11-01
Brand mucus relief
Generic guaifenesin 400 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5cc992c7-a1b3-46be-e053-2991aa0a1f8f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["5b78bbe9-806c-443f-bc23-351e5342355f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-152-01)", "package_ndc": "17714-152-01", "marketing_start_date": "20161101"}], "brand_name": "Mucus Relief", "product_id": "17714-152_5cc992c7-a1b3-46be-e053-2991aa0a1f8f", "dosage_form": "TABLET", "product_ndc": "17714-152", "generic_name": "Guaifenesin 400 mg", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20161101", "listing_expiration_date": "20261231"}