Package 49483-723-50

Brand: guaifenesin extended release 600 mg

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 49483-723-50
Digits Only 4948372350
Product NDC 49483-723
Description

500 TABLET in 1 BOTTLE (49483-723-50)

Marketing

Marketing Status
Marketed Since 2024-01-08
Brand guaifenesin extended release 600 mg
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "10c427f2-f75b-9e93-e063-6294a90ab0ef", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0349483724707", "0349483723502"], "unii": ["495W7451VQ"], "rxcui": ["310621", "636522"], "spl_set_id": ["10c42869-7df0-3046-e063-6394a90aa679"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TIME CAP LABORATORIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (49483-723-50)", "package_ndc": "49483-723-50", "marketing_start_date": "20240108"}], "brand_name": "Guaifenesin Extended Release 600 mg", "product_id": "49483-723_10c427f2-f75b-9e93-e063-6294a90ab0ef", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "49483-723", "generic_name": "Guaifenesin", "labeler_name": "TIME CAP LABORATORIES, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin Extended Release 600 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA217780", "marketing_category": "ANDA", "marketing_start_date": "20240108", "listing_expiration_date": "20261231"}