Package 0220-2952-41
Brand: kali muriaticum
Generic: potassium chloridePackage Facts
Identity
Package NDC
0220-2952-41
Digits Only
0220295241
Product NDC
0220-2952
Description
9 [hp_C] in 1 TUBE (0220-2952-41)
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": "0a0e1894-0bee-949b-e063-6394a90a60a2", "openfda": {"unii": ["660YQ98I10"], "spl_set_id": ["860887e7-7eaf-78c2-e053-2991aa0a9a75"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 [hp_C] in 1 TUBE (0220-2952-41)", "package_ndc": "0220-2952-41", "marketing_start_date": "19830303"}], "brand_name": "Kali muriaticum", "product_id": "0220-2952_0a0e1894-0bee-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": "0220-2952", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali muriaticum", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "9 [hp_C]/9[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}