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 63629-1074
Product ID 63629-1074_9c3f775e-6b6e-41db-828e-6ecb291c8ace
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076368
Listing Expiration 2026-12-31
Marketing Start 2020-06-17

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 636291074
Hyphenated Format 63629-1074

Supplemental Identifiers

RxCUI
1801298
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 ANDA076368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-1)
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-2)
  • 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-3)
source: ndc

Packages (3)

63629-1074-1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-1) 63629-1074-2 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-2) 63629-1074-3 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-3)

Ingredients (1)

potassium chloride (750 mg/1)

Linked Drug Pages (1)

Potassium Chloride Extended-Release ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9c3f775e-6b6e-41db-828e-6ecb291c8ace", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["473369cb-3a9b-437c-b08e-8fb38034c507"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-1)", "package_ndc": "63629-1074-1", "marketing_start_date": "20200617"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-2)", "package_ndc": "63629-1074-2", "marketing_start_date": "20200617"}, {"sample": false, "description": "360 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1074-3)", "package_ndc": "63629-1074-3", "marketing_start_date": "20200617"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "63629-1074_9c3f775e-6b6e-41db-828e-6ecb291c8ace", "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": "63629-1074", "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": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20200617", "listing_expiration_date": "20261231"}