Package 69543-451-10

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 69543-451-10
Digits Only 6954345110
Product NDC 69543-451
Description

100 PACKET in 1 CARTON (69543-451-10) / 1.77 g in 1 PACKET (69543-451-01)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4942d2e3-0d06-4b35-b66b-730fcb9f7bef", "openfda": {"upc": ["0369543451015"], "unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["b43b84ea-babd-477b-b69b-811657bc1503"], "manufacturer_name": ["Virtus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 CARTON (69543-451-10)  / 1.77 g in 1 PACKET (69543-451-01)", "package_ndc": "69543-451-10", "marketing_end_date": "20260831", "marketing_start_date": "20210101"}, {"sample": false, "description": "30 PACKET in 1 CARTON (69543-451-30)  / 1.77 g in 1 PACKET (69543-451-01)", "package_ndc": "69543-451-30", "marketing_end_date": "20260831", "marketing_start_date": "20210101"}], "brand_name": "Potassium Chloride", "product_id": "69543-451_4942d2e3-0d06-4b35-b66b-730fcb9f7bef", "dosage_form": "POWDER, FOR SOLUTION", "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": "69543-451", "generic_name": "Potassium Chloride", "labeler_name": "Virtus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.77g"}], "application_number": "ANDA210200", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20210101"}