potassium chloride

Generic: potassium chloride

Labeler: granules pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler granules pharmaceuticals inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 40 meq/15mL

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-073
Product ID 70010-073_44f3fc8c-926c-1505-e063-6294a90a88fd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213392
Listing Expiration 2026-12-31
Marketing Start 2021-04-25

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 70010073
Hyphenated Format 70010-073

Supplemental Identifiers

RxCUI
312515 314182
UPC
0370010073449 0370010072442
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 ANDA213392 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/15mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (70010-073-44)
source: ndc

Packages (1)

70010-073-44 473 mL in 1 BOTTLE (70010-073-44)

Ingredients (1)

potassium chloride (40 meq/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": "44f3fc8c-926c-1505-e063-6294a90a88fd", "openfda": {"upc": ["0370010073449", "0370010072442"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["302b3fa7-ea87-4bf1-aae0-6a2d7459de86"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (70010-073-44)", "package_ndc": "70010-073-44", "marketing_start_date": "20210425"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "70010-073_44f3fc8c-926c-1505-e063-6294a90a88fd", "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": "70010-073", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/15mL"}], "application_number": "ANDA213392", "marketing_category": "ANDA", "marketing_start_date": "20210425", "listing_expiration_date": "20261231"}