potassium chloride

Generic: potassium chloride

Labeler: dr. reddys laboratories, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride
Labeler dr. reddys laboratories, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 40 meq/30mL

Manufacturer
Dr. Reddys Laboratories, Inc.

Identifiers & Regulatory

Product NDC 43598-160
Product ID 43598-160_21ff31d2-239a-4997-b999-3b7cc55994b9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213062
Listing Expiration 2026-12-31
Marketing Start 2022-07-25

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 43598160
Hyphenated Format 43598-160

Supplemental Identifiers

RxCUI
312515
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 ANDA213062 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 meq/30mL
source: ndc
Packaging
  • 100 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-01) / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)
  • 50 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-53) / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)
source: ndc

Packages (2)

43598-160-01 100 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-01) / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31) 43598-160-53 50 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-53) / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)

Ingredients (1)

potassium chloride (40 meq/30mL)

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21ff31d2-239a-4997-b999-3b7cc55994b9", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515"], "spl_set_id": ["dda82a38-0c08-4947-99b7-915c2949bf16"], "manufacturer_name": ["Dr. Reddys Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-01)  / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)", "package_ndc": "43598-160-01", "marketing_start_date": "20220725"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 PACKAGE (43598-160-53)  / 30 mL in 1 CUP, UNIT-DOSE (43598-160-31)", "package_ndc": "43598-160-53", "marketing_start_date": "20220725"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "43598-160_21ff31d2-239a-4997-b999-3b7cc55994b9", "dosage_form": "SOLUTION", "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": "43598-160", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Dr. Reddys Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "40 meq/30mL"}], "application_number": "ANDA213062", "marketing_category": "ANDA", "marketing_start_date": "20220725", "listing_expiration_date": "20261231"}