potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 1.5 g/1.56g

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-197
Product ID 70954-197_0128a879-7185-4b70-b0bb-d108ff1c9542
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212816
Listing Expiration 2026-12-31
Marketing Start 2023-07-19

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 70954197
Hyphenated Format 70954-197

Supplemental Identifiers

RxCUI
1867544
UPC
0370954197102
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 ANDA212816 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/1.56g
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (70954-197-20) / 1.56 g in 1 POUCH (70954-197-10)
  • 100 POUCH in 1 CARTON (70954-197-30) / 1.56 g in 1 POUCH (70954-197-10)
source: ndc

Packages (2)

70954-197-20 30 POUCH in 1 CARTON (70954-197-20) / 1.56 g in 1 POUCH (70954-197-10) 70954-197-30 100 POUCH in 1 CARTON (70954-197-30) / 1.56 g in 1 POUCH (70954-197-10)

Ingredients (1)

potassium chloride (1.5 g/1.56g)

Linked Drug Pages (1)

Potassium chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0128a879-7185-4b70-b0bb-d108ff1c9542", "openfda": {"upc": ["0370954197102"], "unii": ["660YQ98I10"], "rxcui": ["1867544"], "spl_set_id": ["0128a879-7185-4b70-b0bb-d108ff1c9542"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (70954-197-20)  / 1.56 g in 1 POUCH (70954-197-10)", "package_ndc": "70954-197-20", "marketing_start_date": "20230719"}, {"sample": false, "description": "100 POUCH in 1 CARTON (70954-197-30)  / 1.56 g in 1 POUCH (70954-197-10)", "package_ndc": "70954-197-30", "marketing_start_date": "20230719"}], "brand_name": "Potassium chloride", "product_id": "70954-197_0128a879-7185-4b70-b0bb-d108ff1c9542", "dosage_form": "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": "70954-197", "generic_name": "Potassium chloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/1.56g"}], "application_number": "ANDA212816", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}