Package 0574-0601-15

Brand: podocon 25

Generic: podophyllum resin
NDC Package

Package Facts

Identity

Package NDC 0574-0601-15
Digits Only 0574060115
Product NDC 0574-0601
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0601-15) / 15 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 1990-09-01
Brand podocon 25
Generic podophyllum resin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "e2ac9612-bded-4eea-a664-f941416583fa", "openfda": {"unii": ["16902YVY2B"], "spl_set_id": ["de96dc6e-e6d1-4383-9ce1-4d06bac08e00"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (0574-0601-15)  / 15 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "0574-0601-15", "marketing_start_date": "19900901"}], "brand_name": "Podocon 25", "product_id": "0574-0601_e2ac9612-bded-4eea-a664-f941416583fa", "dosage_form": "TINCTURE", "product_ndc": "0574-0601", "generic_name": "Podophyllum resin", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Podocon 25", "active_ingredients": [{"name": "PODOPHYLLUM RESIN", "strength": "1 mg/4mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "19900901", "listing_expiration_date": "20261231"}