Package 0220-2978-41

Brand: kali sulphuricum

Generic: potassium sulfate
NDC Package

Package Facts

Identity

Package NDC 0220-2978-41
Digits Only 0220297841
Product NDC 0220-2978
Description

200 [kp_C] in 1 TUBE (0220-2978-41)

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": "f2b90b86-d09e-7a52-e053-2995a90ab95b", "openfda": {"unii": ["1K573LC5TV"], "spl_set_id": ["860b8433-1162-6c82-e053-2a91aa0a7bbf"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 [kp_C] in 1 TUBE (0220-2978-41)", "package_ndc": "0220-2978-41", "marketing_start_date": "19830303"}], "brand_name": "Kali sulphuricum", "product_id": "0220-2978_f2b90b86-d09e-7a52-e053-2995a90ab95b", "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": "0220-2978", "generic_name": "POTASSIUM SULFATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali sulphuricum", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "200 [kp_C]/200[kp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}