Package 0220-4127-41

Brand: podophyllum peltatum

Generic: podophyllum
NDC Package

Package Facts

Identity

Package NDC 0220-4127-41
Digits Only 0220412741
Product NDC 0220-4127
Description

6 [hp_C] in 1 TUBE (0220-4127-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand podophyllum peltatum
Generic podophyllum
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f2f5949e-4482-2724-e053-2a95a90a9f9a", "openfda": {"unii": ["2S713A4VP3"], "spl_set_id": ["86a6c6af-8699-edbc-e053-2991aa0aaa24"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 [hp_C] in 1 TUBE (0220-4127-41)", "package_ndc": "0220-4127-41", "marketing_start_date": "19830303"}], "brand_name": "Podophyllum peltatum", "product_id": "0220-4127_f2f5949e-4482-2724-e053-2a95a90a9f9a", "dosage_form": "PELLET", "product_ndc": "0220-4127", "generic_name": "PODOPHYLLUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Podophyllum peltatum", "active_ingredients": [{"name": "PODOPHYLLUM", "strength": "6 [hp_C]/6[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}