potassium chloride extended-release

Generic: potassium chloride

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride extended-release
Generic Name potassium chloride
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 63304-076
Product ID 63304-076_0e924cf6-53b8-28c4-e063-6294a90a4ac4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076368
Listing Expiration 2026-12-31
Marketing Start 2019-11-20

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 63304076
Hyphenated Format 63304-076

Supplemental Identifiers

RxCUI
1801298
UPC
0363304076011
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 ANDA076368 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-01)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-05)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-10)
source: ndc

Packages (3)

63304-076-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-01) 63304-076-05 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-05) 63304-076-10 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-10)

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": "0e924cf6-53b8-28c4-e063-6294a90a4ac4", "openfda": {"upc": ["0363304076011"], "unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["8ed8ea55-8b15-f718-e053-2a95a90a587a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-01)", "package_ndc": "63304-076-01", "marketing_start_date": "20191120"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-05)", "package_ndc": "63304-076-05", "marketing_start_date": "20191120"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-076-10)", "package_ndc": "63304-076-10", "marketing_start_date": "20191120"}], "brand_name": "Potassium Chloride Extended-Release", "product_id": "63304-076_0e924cf6-53b8-28c4-e063-6294a90a4ac4", "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": "63304-076", "generic_name": "Potassium Chloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "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": "20191120", "listing_expiration_date": "20261231"}