potassium chloride (69543-451)

Drug Facts

Product Profile

Brand Name potassium chloride

Generic Name potassium chloride

Labeler virtus pharmaceuticals, llc

Dosage Form POWDER, FOR SOLUTION

Routes

ORAL

Active Ingredients

potassium chloride 1.5 g/1.77g

Manufacturer

Virtus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69543-451

Product ID 69543-451_4942d2e3-0d06-4b35-b66b-730fcb9f7bef

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA210200

Marketing Start 2021-01-01

Marketing End 2026-08-31

Pharmacologic Class

Classes

increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69543451

Hyphenated Format 69543-451

Supplemental Identifiers

RxCUI

1867544

UPC

0369543451015

UNII

660YQ98I10

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name potassium chloride (source: ndc)

Generic Name potassium chloride (source: ndc)

Application Number ANDA210200 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

1.5 g/1.77g

source: ndc

Packaging

100 PACKET in 1 CARTON (69543-451-10) / 1.77 g in 1 PACKET (69543-451-01)
30 PACKET in 1 CARTON (69543-451-30) / 1.77 g in 1 PACKET (69543-451-01)

source: ndc

Packages (2)

69543-451-10 100 PACKET in 1 CARTON (69543-451-10) / 1.77 g in 1 PACKET (69543-451-01) 69543-451-30 30 PACKET in 1 CARTON (69543-451-30) / 1.77 g in 1 PACKET (69543-451-01)

Ingredients (1)

potassium chloride (1.5 g/1.77g)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

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"}