Package 0220-2837-41
Brand: kali bichromicum
Generic: potassium dichromatePackage Facts
Identity
Package NDC
0220-2837-41
Digits Only
0220283741
Product NDC
0220-2837
Description
30 [hp_X] in 1 TUBE (0220-2837-41)
Marketing
Marketing Status
Brand
kali bichromicum
Generic
potassium dichromate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0dfe8a-78d6-8525-e063-6394a90aff46", "openfda": {"unii": ["T4423S18FM"], "spl_set_id": ["860669cb-694b-c98d-e053-2991aa0aa0e3"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_X] in 1 TUBE (0220-2837-41)", "package_ndc": "0220-2837-41", "marketing_start_date": "19830303"}], "brand_name": "Kali bichromicum", "product_id": "0220-2837_0a0dfe8a-78d6-8525-e063-6394a90aff46", "dosage_form": "PELLET", "product_ndc": "0220-2837", "generic_name": "POTASSIUM DICHROMATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali bichromicum", "active_ingredients": [{"name": "POTASSIUM DICHROMATE", "strength": "30 [hp_X]/30[hp_X]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}