potassium chloride extended release

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 750 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-022
Product ID 70010-022_f33d5a34-e5e7-a85f-e053-2995a90a6db3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211797
Listing Expiration 2026-12-31
Marketing Start 2020-10-22

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 70010022
Hyphenated Format 70010-022

Supplemental Identifiers

RxCUI
312529 628953
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 extended release (source: ndc)
Generic Name potassium chloride (source: ndc)
Application Number ANDA211797 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-05)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-10)
  • 3 BLISTER PACK in 1 CARTON (70010-022-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 10 BLISTER PACK in 1 CARTON (70010-022-62) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (5)

70010-022-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-01) 70010-022-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-05) 70010-022-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-10) 70010-022-61 3 BLISTER PACK in 1 CARTON (70010-022-61) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK 70010-022-62 10 BLISTER PACK in 1 CARTON (70010-022-62) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

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": "f33d5a34-e5e7-a85f-e053-2995a90a6db3", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["9f8d2886-9ecd-4cbf-a84a-2d221cb3497c"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-01)", "package_ndc": "70010-022-01", "marketing_start_date": "20201022"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-05)", "package_ndc": "70010-022-05", "marketing_start_date": "20201022"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-022-10)", "package_ndc": "70010-022-10", "marketing_start_date": "20210504"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70010-022-61)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70010-022-61", "marketing_start_date": "20220103"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70010-022-62)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70010-022-62", "marketing_start_date": "20220103"}], "brand_name": "POTASSIUM CHLORIDE EXTENDED RELEASE", "product_id": "70010-022_f33d5a34-e5e7-a85f-e053-2995a90a6db3", "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": "70010-022", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE EXTENDED RELEASE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA211797", "marketing_category": "ANDA", "marketing_start_date": "20201022", "listing_expiration_date": "20261231"}