potassium chloride extended release

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride extended release
Generic Name potassium chloride
Labeler bryant ranch prepack
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-8442
Product ID 63629-8442_e26d6cbc-1dbc-4d6b-b60a-24d62e6d0958
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205993
Listing Expiration 2026-12-31
Marketing Start 2015-12-11

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 636298442
Hyphenated Format 63629-8442

Supplemental Identifiers

RxCUI
628953
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 extended release (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA205993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8442-1)
source: ndc

Packages (1)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e26d6cbc-1dbc-4d6b-b60a-24d62e6d0958", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["41ff55cf-4af3-487e-bd78-09703d310780"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8442-1)", "package_ndc": "63629-8442-1", "marketing_start_date": "20151218"}], "brand_name": "Potassium chloride extended release", "product_id": "63629-8442_e26d6cbc-1dbc-4d6b-b60a-24d62e6d0958", "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": "63629-8442", "generic_name": "Potassium chloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium chloride extended release", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA205993", "marketing_category": "ANDA", "marketing_start_date": "20151211", "listing_expiration_date": "20261231"}