Package 0220-2891-41
Brand: kali muriaticum
Generic: potassium chloridePackage Facts
Identity
Package NDC
0220-2891-41
Digits Only
0220289141
Product NDC
0220-2891
Description
80 PELLET in 1 TUBE (0220-2891-41)
Marketing
Marketing Status
Brand
kali muriaticum
Generic
potassium chloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "07d90edc-88ec-06a4-e063-6294a90ae585", "openfda": {"unii": ["660YQ98I10"], "spl_set_id": ["caaad470-7be1-11e6-b409-424c58303031"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 PELLET in 1 TUBE (0220-2891-41)", "package_ndc": "0220-2891-41", "marketing_start_date": "19830303"}], "brand_name": "Kali muriaticum", "product_id": "0220-2891_07d90edc-88ec-06a4-e063-6294a90ae585", "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": "0220-2891", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali muriaticum", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}