Package 68001-561-17

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 68001-561-17
Digits Only 6800156117
Product NDC 68001-561
Product ID 68001-561_0c4ee6ca-2596-fbd2-e063-6394a90a0806
Description

8 BLISTER PACK in 1 CARTON (68001-561-17) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16)

Marketing

Marketing Status
Marketed Since 2023-03-15
Brand guaifenesin
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Guaifenesin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c4ee6ca-2596-fbd2-e063-6394a90a0806", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["ee8a2a97-16aa-0f3e-e053-2a95a90a523b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 BLISTER PACK in 1 CARTON (68001-561-17)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68001-561-16)", "package_ndc": "68001-561-17", "marketing_start_date": "20230315"}], "brand_name": "Guaifenesin", "product_id": "68001-561_0c4ee6ca-2596-fbd2-e063-6394a90a0806", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "68001-561", "generic_name": "Guaifenesin", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA210453", "marketing_category": "ANDA", "marketing_start_date": "20230315", "listing_expiration_date": "20261231"}