Package 54973-5230-1

Brand: kali sulph

Generic: potassium sulfate
NDC Package

Package Facts

Identity

Package NDC 54973-5230-1
Digits Only 5497352301
Product NDC 54973-5230
Product ID 54973-5230_f0330ffb-503d-2671-e053-2995a90a8218
Description

500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1)

Marketing

Marketing Status
Marketed Since 1940-01-01
Brand kali sulph
Generic potassium sulfate
Sample Package No

Linked Drug Pages (1)

KALI SULPH ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f0330ffb-503d-2671-e053-2995a90a8218", "openfda": {"upc": ["0354973523012"], "unii": ["1K573LC5TV"], "spl_set_id": ["c00e31d8-76df-47b1-bafd-36d088395522"], "manufacturer_name": ["Hyland's Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (54973-5230-1)", "package_ndc": "54973-5230-1", "marketing_start_date": "19400101"}], "brand_name": "KALI SULPH", "product_id": "54973-5230_f0330ffb-503d-2671-e053-2995a90a8218", "dosage_form": "TABLET", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "54973-5230", "generic_name": "potassium sulfate", "labeler_name": "Hyland's Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "KALI SULPH", "active_ingredients": [{"name": "POTASSIUM SULFATE", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19400101", "listing_expiration_date": "20261231"}