Package 0220-2974-41

Brand: kali sulphuricum

Generic: potassium sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-2974-41
Digits Only 0220297441
Product NDC 0220-2974
Description

9 [hp_C] in 1 TUBE (0220-2974-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand kali sulphuricum
Generic potassium sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1894-0bf1-949b-e063-6394a90a60a2", "openfda": {"unii": ["1K573LC5TV"], "spl_set_id": ["860b1099-8939-cfad-e053-2991aa0a5ebc"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2974-41)", "package_ndc": "0220-2974-41", "marketing_start_date": "19830303"}], "brand_name": "Kali sulphuricum", "product_id": "0220-2974_0a0e1894-0bf1-949b-e063-6394a90a60a2", "dosage_form": "PELLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0220-2974", "generic_name": "POTASSIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}