potassium chloride

Generic: potassium chloride

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

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler granules pharmaceuticals inc
Dosage Form CAPSULE, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 600 mg/1

Manufacturer
Granules Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 70010-147
Product ID 70010-147_495d6938-4058-2799-e063-6294a90adc8f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214686
Listing Expiration 2027-12-31
Marketing Start 2021-03-01

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 70010147
Hyphenated Format 70010-147

Supplemental Identifiers

RxCUI
312504 315183
UPC
0370010148017 0370010147010
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 ANDA214686 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-147-01)
source: ndc

Packages (1)

70010-147-01 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-147-01)

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": "495d6938-4058-2799-e063-6294a90adc8f", "openfda": {"upc": ["0370010148017", "0370010147010"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["c1f4832d-4d5c-8c49-e053-2a95a90ac9fe"], "manufacturer_name": ["Granules Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-147-01)", "package_ndc": "70010-147-01", "marketing_start_date": "20210301"}], "brand_name": "Potassium Chloride", "product_id": "70010-147_495d6938-4058-2799-e063-6294a90adc8f", "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": "70010-147", "generic_name": "Potassium Chloride", "labeler_name": "Granules Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA214686", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20271231"}