Package 25000-042-55

Brand: guaifenesin 600 mg

Generic: guaifenesin 600 mg
NDC Package

Package Facts

Identity

Package NDC 25000-042-55
Digits Only 2500004255
Product NDC 25000-042
Description

2 BLISTER PACK in 1 CARTON (25000-042-55) / 10 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-08-23
Brand guaifenesin 600 mg
Generic guaifenesin 600 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0af3bdb4-c1f3-4941-a1de-6e08c49849cb", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0325000042127", "0325000041120", "0325000042554", "0325000041342", "0325000041755", "0325000042011", "0325000042998"], "unii": ["495W7451VQ"], "rxcui": ["310621", "636522"], "spl_set_id": ["fedf43d0-d6d1-4f50-bbab-396701e45cb2"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["MARKSANS PHARMA LIMITED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (25000-042-01)  / 20 TABLET in 1 BOTTLE", "package_ndc": "25000-042-01", "marketing_start_date": "20230823"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (25000-042-12)", "package_ndc": "25000-042-12", "marketing_start_date": "20230823"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (25000-042-55)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "25000-042-55", "marketing_start_date": "20230823"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (25000-042-99)  / 20 TABLET in 1 BLISTER PACK", "package_ndc": "25000-042-99", "marketing_start_date": "20250418"}], "brand_name": "Guaifenesin 600 mg", "product_id": "25000-042_0af3bdb4-c1f3-4941-a1de-6e08c49849cb", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "25000-042", "generic_name": "Guaifenesin 600 mg", "labeler_name": "MARKSANS PHARMA LIMITED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin 600 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA217780", "marketing_category": "ANDA", "marketing_start_date": "20230823", "listing_expiration_date": "20261231"}