Package 69848-017-02

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 69848-017-02
Digits Only 6984801702
Product NDC 69848-017
Description

20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)

Marketing

Marketing Status
Marketed Since 2022-01-06
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": "46909531-34b7-b81b-e063-6394a90a8515", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["a62d427e-f339-f225-e053-2a95a90ab387"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["GRANULES USA, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (69848-017-02)", "package_ndc": "69848-017-02", "marketing_start_date": "20220106"}], "brand_name": "Guaifenesin", "product_id": "69848-017_46909531-34b7-b81b-e063-6394a90a8515", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "69848-017", "generic_name": "Guaifenesin", "labeler_name": "GRANULES USA, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20211231", "listing_expiration_date": "20261231"}