potassium chloride

Generic: potassium chloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler bryant ranch prepack
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/1.77g

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2310
Product ID 72162-2310_d914b262-7244-4d71-980d-e5508f994eba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210200
Listing Expiration 2026-12-31
Marketing Start 2021-01-01

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 721622310
Hyphenated Format 72162-2310

Supplemental Identifiers

RxCUI
1867544
UNII
660YQ98I10

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 (72162-2310-1) / 1.77 g in 1 PACKET (72162-2310-2)
  • 30 PACKET in 1 CARTON (72162-2310-3) / 1.77 g in 1 PACKET (72162-2310-4)
source: ndc

Packages (2)

72162-2310-1 100 PACKET in 1 CARTON (72162-2310-1) / 1.77 g in 1 PACKET (72162-2310-2) 72162-2310-3 30 PACKET in 1 CARTON (72162-2310-3) / 1.77 g in 1 PACKET (72162-2310-4)

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": "d914b262-7244-4d71-980d-e5508f994eba", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["7a220e87-ff72-417b-bc45-90a37b7f2aa6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 CARTON (72162-2310-1)  / 1.77 g in 1 PACKET (72162-2310-2)", "package_ndc": "72162-2310-1", "marketing_start_date": "20240507"}, {"sample": false, "description": "30 PACKET in 1 CARTON (72162-2310-3)  / 1.77 g in 1 PACKET (72162-2310-4)", "package_ndc": "72162-2310-3", "marketing_start_date": "20240507"}], "brand_name": "Potassium Chloride", "product_id": "72162-2310_d914b262-7244-4d71-980d-e5508f994eba", "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": "72162-2310", "generic_name": "Potassium Chloride", "labeler_name": "Bryant Ranch Prepack", "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_start_date": "20210101", "listing_expiration_date": "20261231"}