Package 0574-0521-74

Brand: actidose aqua

Generic: activated charcoal
NDC Package

Package Facts

Identity

Package NDC 0574-0521-74
Digits Only 0574052174
Product NDC 0574-0521
Description

120 mL in 1 TUBE (0574-0521-74)

Marketing

Marketing Status
Marketed Since 2020-11-10
Brand actidose aqua
Generic activated charcoal
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c576120d-0764-479c-9a39-c6e42d3ac8c1", "openfda": {"unii": ["2P3VWU3H10"], "rxcui": ["309150", "1251411"], "spl_set_id": ["c85dc235-3f42-4361-9bd2-1aaff798ad75"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (0574-0521-04)", "package_ndc": "0574-0521-04", "marketing_start_date": "20201111"}, {"sample": false, "description": "240 mL in 1 BOTTLE (0574-0521-08)", "package_ndc": "0574-0521-08", "marketing_start_date": "20201111"}, {"sample": false, "description": "72 mL in 1 TUBE (0574-0521-25)", "package_ndc": "0574-0521-25", "marketing_start_date": "20230131"}, {"sample": false, "description": "120 mL in 1 TUBE (0574-0521-74)", "package_ndc": "0574-0521-74", "marketing_start_date": "20201110"}, {"sample": false, "description": "240 mL in 1 TUBE (0574-0521-76)", "package_ndc": "0574-0521-76", "marketing_start_date": "20201213"}], "brand_name": "ACTIDOSE AQUA", "product_id": "0574-0521_c576120d-0764-479c-9a39-c6e42d3ac8c1", "dosage_form": "SUSPENSION", "product_ndc": "0574-0521", "generic_name": "activated charcoal", "labeler_name": "Padagis US LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACTIDOSE AQUA", "active_ingredients": [{"name": "ACTIVATED CHARCOAL", "strength": "208 mg/mL"}], "application_number": "M023", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201110", "listing_expiration_date": "20261231"}