Package 0220-2957-41

Brand: kali muriaticum

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0220-2957-41
Digits Only 0220295741
Product NDC 0220-2957
Description

1 [hp_M] in 1 TUBE (0220-2957-41)

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": "0a0dfe8a-78da-8525-e063-6394a90aff46", "openfda": {"unii": ["660YQ98I10"], "spl_set_id": ["86090ebb-0fb2-2c9c-e053-2a91aa0a0561"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 [hp_M] in 1 TUBE (0220-2957-41)", "package_ndc": "0220-2957-41", "marketing_start_date": "19830303"}], "brand_name": "Kali muriaticum", "product_id": "0220-2957_0a0dfe8a-78da-8525-e063-6394a90aff46", "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": "0220-2957", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali muriaticum", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1 [hp_M]/[hp_M]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}