Package 0220-4136-41

Brand: podophyllum peltatum

Generic: podophyllum
NDC Package

Package Facts

Identity

Package NDC 0220-4136-41
Digits Only 0220413641
Product NDC 0220-4136
Description

30 [hp_C] in 1 TUBE (0220-4136-41)

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": "f67d6f73-88d5-2031-e053-2995a90a3b09", "openfda": {"unii": ["2S713A4VP3"], "spl_set_id": ["86a71607-d6cd-28ff-e053-2991aa0a37e4"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-4136-41)", "package_ndc": "0220-4136-41", "marketing_start_date": "19830303"}], "brand_name": "Podophyllum peltatum", "product_id": "0220-4136_f67d6f73-88d5-2031-e053-2995a90a3b09", "dosage_form": "PELLET", "product_ndc": "0220-4136", "generic_name": "PODOPHYLLUM", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Podophyllum peltatum", "active_ingredients": [{"name": "PODOPHYLLUM", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}