potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-133
Product ID 31722-133_54ef7636-02b5-4062-9171-625d089ebfce
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214422
Listing Expiration 2026-12-31
Marketing Start 2021-01-20

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 31722133
Hyphenated Format 31722-133

Supplemental Identifiers

RxCUI
403888 1801294 1801298
UPC
0331722135016 0331722135054 0331722134019 0331722133012 0331722133050
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 ANDA214422 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)
source: ndc

Packages (2)

31722-133-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01) 31722-133-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "54ef7636-02b5-4062-9171-625d089ebfce", "openfda": {"upc": ["0331722135016", "0331722135054", "0331722134019", "0331722133012", "0331722133050"], "unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["b1e827aa-b2fb-4fa5-984d-ddd94338ff53"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-01)", "package_ndc": "31722-133-01", "marketing_start_date": "20210120"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-133-05)", "package_ndc": "31722-133-05", "marketing_start_date": "20210120"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "31722-133_54ef7636-02b5-4062-9171-625d089ebfce", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "31722-133", "generic_name": "Potassium CHLORIDE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}