Package 0220-2955-41

Brand: kali muriaticum

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0220-2955-41
Digits Only 0220295541
Product NDC 0220-2955
Description

30 [hp_C] in 1 TUBE (0220-2955-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
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": "f2f668b5-5047-5e26-e053-2a95a90a106d", "openfda": {"unii": ["660YQ98I10"], "spl_set_id": ["8608d5a3-93e6-e8e2-e053-2a91aa0aaedc"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 [hp_C] in 1 TUBE (0220-2955-41)", "package_ndc": "0220-2955-41", "marketing_start_date": "19830303"}], "brand_name": "Kali muriaticum", "product_id": "0220-2955_f2f668b5-5047-5e26-e053-2a95a90a106d", "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": "0220-2955", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali muriaticum", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "30 [hp_C]/30[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}