potassium chloride

Generic: potassium chloride oral

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride oral
Labeler atlantic biologicals corp.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/15mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-0048
Product ID 17856-0048_45af915d-a3d7-b59a-e063-6294a90ac162
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211648
Listing Expiration 2026-12-31
Marketing Start 2023-10-05

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 178560048
Hyphenated Format 17856-0048

Supplemental Identifiers

RxCUI
312515
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 oral (source: ndc)
Application Number ANDA211648 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/15mL
source: ndc
Packaging
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-0048-2)
  • 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-3) / 30 mL in 1 CUP, UNIT-DOSE (17856-0048-4)
source: ndc

Packages (2)

17856-0048-1 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-1) / 15 mL in 1 CUP, UNIT-DOSE (17856-0048-2) 17856-0048-3 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-3) / 30 mL in 1 CUP, UNIT-DOSE (17856-0048-4)

Ingredients (1)

potassium chloride (1.5 g/15mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45af915d-a3d7-b59a-e063-6294a90ac162", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["dc55474c-cc51-4f17-8cb3-0f34b3e68a55"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-1)  / 15 mL in 1 CUP, UNIT-DOSE (17856-0048-2)", "package_ndc": "17856-0048-1", "marketing_start_date": "20240711"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0048-3)  / 30 mL in 1 CUP, UNIT-DOSE (17856-0048-4)", "package_ndc": "17856-0048-3", "marketing_start_date": "20240711"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "17856-0048_45af915d-a3d7-b59a-e063-6294a90ac162", "dosage_form": "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": "17856-0048", "generic_name": "POTASSIUM CHLORIDE ORAL", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/15mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20231005", "listing_expiration_date": "20261231"}