potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

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

potassium chloride 600 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 63304-078
Product ID 63304-078_0e920885-4086-c99c-e063-6294a90aaa67
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208864
Listing Expiration 2026-12-31
Marketing Start 2020-01-02

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 63304078
Hyphenated Format 63304-078

Supplemental Identifiers

RxCUI
312504 315183
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 ANDA208864 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-078-01)
source: ndc

Packages (1)

63304-078-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-078-01)

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": "0e920885-4086-c99c-e063-6294a90aaa67", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["4d90d03d-7f0e-4d49-9e80-628dbc7165c0"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-078-01)", "package_ndc": "63304-078-01", "marketing_start_date": "20200102"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "63304-078_0e920885-4086-c99c-e063-6294a90aaa67", "dosage_form": "CAPSULE, 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": "63304-078", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA208864", "marketing_category": "ANDA", "marketing_start_date": "20200102", "listing_expiration_date": "20261231"}