Package 51660-567-54
Brand: guaifenesin
Generic: guaifenesinPackage Facts
Identity
Package NDC
51660-567-54
Digits Only
5166056754
Product NDC
51660-567
Description
14 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-54)
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": "4aa4fb35-6f33-6e33-e063-6394a90a495e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621", "636522"], "spl_set_id": ["7076e42a-17ff-4c42-9963-2dc02c0a5e49"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Ohm Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-54)", "package_ndc": "51660-567-54", "marketing_start_date": "20220401"}, {"sample": false, "description": "56 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-58)", "package_ndc": "51660-567-58", "marketing_start_date": "20220401"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 CARTON (51660-567-86)", "package_ndc": "51660-567-86", "marketing_start_date": "20220401"}], "brand_name": "Guaifenesin", "product_id": "51660-567_4aa4fb35-6f33-6e33-e063-6394a90a495e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "51660-567", "generic_name": "Guaifenesin", "labeler_name": "Ohm Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA209254", "marketing_category": "ANDA", "marketing_start_date": "20220401", "listing_expiration_date": "20271231"}