Package 0220-2921-41

Brand: kali sulphuricum

Generic: potassium sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-2921-41
Digits Only 0220292141
Product NDC 0220-2921
Description

80 PELLET in 1 TUBE (0220-2921-41)

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": "0a0e390d-fe5d-9dc6-e063-6294a90a5f58", "openfda": {"unii": ["1K573LC5TV"], "spl_set_id": ["880ebaa0-7be6-11e6-8197-424c58303031"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 TUBE (0220-2921-41)", "package_ndc": "0220-2921-41", "marketing_start_date": "19830303"}], "brand_name": "Kali sulphuricum", "product_id": "0220-2921_0a0e390d-fe5d-9dc6-e063-6294a90a5f58", "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": "0220-2921", "generic_name": "POTASSIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}