Package 0574-0621-05

Brand: podofilox

Generic: podofilox
NDC Package

Package Facts

Identity

Package NDC 0574-0621-05
Digits Only 0574062105
Product NDC 0574-0621
Product ID 0574-0621_d2e70c5e-d4a9-4295-9eff-517ffb974e61
Description

3.5 g in 1 TUBE, WITH APPLICATOR (0574-0621-05)

Marketing

Marketing Status
Marketed Since 2023-12-13
Brand podofilox
Generic podofilox
Sample Package No

Linked Drug Pages (1)

Podofilox ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "d2e70c5e-d4a9-4295-9eff-517ffb974e61", "openfda": {"nui": ["N0000008732"], "unii": ["L36H50F353"], "rxcui": ["312466"], "spl_set_id": ["d2e70c5e-d4a9-4295-9eff-517ffb974e61"], "pharm_class_pe": ["Decreased Mitosis [PE]"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3.5 g in 1 TUBE, WITH APPLICATOR (0574-0621-05)", "package_ndc": "0574-0621-05", "marketing_start_date": "20231213"}], "brand_name": "Podofilox", "product_id": "0574-0621_d2e70c5e-d4a9-4295-9eff-517ffb974e61", "dosage_form": "GEL", "pharm_class": ["Decreased Mitosis [PE]"], "product_ndc": "0574-0621", "generic_name": "Podofilox", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Podofilox", "active_ingredients": [{"name": "PODOFILOX", "strength": "5 mg/g"}], "application_number": "ANDA211871", "marketing_category": "ANDA", "marketing_start_date": "20231213", "listing_expiration_date": "20261231"}