potassium chloride

Generic: potassium chloride

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler zydus lifesciences limited
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

potassium chloride 750 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1599
Product ID 70771-1599_c6b38e40-cd5a-41ed-92d6-eb25e9c0c725
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210395
Listing Expiration 2026-12-31
Marketing Start 2022-02-03

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 707711599
Hyphenated Format 70771-1599

Supplemental Identifiers

RxCUI
1801294 1801298
UPC
0370771160013 0370771159918
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 ANDA210395 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-0)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-1)
source: ndc

Packages (2)

70771-1599-0 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-0) 70771-1599-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-1)

Ingredients (1)

potassium chloride (750 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": "c6b38e40-cd5a-41ed-92d6-eb25e9c0c725", "openfda": {"upc": ["0370771160013", "0370771159918"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["099c3a36-f460-4191-80e5-0c4153a5c713"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-0)", "package_ndc": "70771-1599-0", "marketing_start_date": "20220203"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1599-1)", "package_ndc": "70771-1599-1", "marketing_start_date": "20220203"}], "brand_name": "Potassium Chloride", "product_id": "70771-1599_c6b38e40-cd5a-41ed-92d6-eb25e9c0c725", "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": "70771-1599", "generic_name": "Potassium Chloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA210395", "marketing_category": "ANDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}