potassium chloride

Generic: potassium chloride

Labeler: strides pharma science limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler strides pharma science limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
Strides Pharma Science Limited

Identifiers & Regulatory

Product NDC 64380-860
Product ID 64380-860_a74390de-64e9-482d-8630-d1a2452324fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210733
Listing Expiration 2026-12-31
Marketing Start 2018-11-19

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 64380860
Hyphenated Format 64380-860

Supplemental Identifiers

RxCUI
312529 628953
UPC
0364380861065 0364380860068
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 ANDA210733 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-07)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-08)
source: ndc

Packages (3)

64380-860-06 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06) 64380-860-07 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-07) 64380-860-08 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-08)

Ingredients (1)

potassium chloride (600 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": "a74390de-64e9-482d-8630-d1a2452324fe", "openfda": {"upc": ["0364380861065", "0364380860068"], "unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["0224e5b3-3c49-4e6e-aa78-1abcc6969246"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-06)", "package_ndc": "64380-860-06", "marketing_start_date": "20181119"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-07)", "package_ndc": "64380-860-07", "marketing_start_date": "20181127"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (64380-860-08)", "package_ndc": "64380-860-08", "marketing_start_date": "20181127"}], "brand_name": "Potassium Chloride", "product_id": "64380-860_a74390de-64e9-482d-8630-d1a2452324fe", "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": "64380-860", "generic_name": "Potassium Chloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA210733", "marketing_category": "ANDA", "marketing_start_date": "20181119", "listing_expiration_date": "20261231"}