Potassium Chloride

Generic: Potassium Chloride

Labeler: Strides Pharma Science Limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Potassium Chloride
Generic Name Potassium Chloride
Labeler Strides Pharma Science Limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

POTASSIUM CHLORIDE 20 meq/15mL

Identifiers & Regulatory

Product NDC 64380-873
Product ID 64380-873_58d1944f-cc5c-4cac-b559-f77fdb5c4f0c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211665
Listing Expiration 2026-12-31
Marketing Start 2025-08-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64380873
Hyphenated Format 64380-873

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 ANDA211665 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 meq/15mL
source: ndc
Packaging
  • 10 CUP, UNIT-DOSE in 1 TRAY (64380-873-59) / 30 mL in 1 CUP, UNIT-DOSE
  • 473 mL in 1 BOTTLE, PLASTIC (64380-873-71)
  • 10 CUP, UNIT-DOSE in 1 TRAY (64380-873-91) / 15 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (3)

64380-873-59 10 CUP, UNIT-DOSE in 1 TRAY (64380-873-59) / 30 mL in 1 CUP, UNIT-DOSE 64380-873-71 473 mL in 1 BOTTLE, PLASTIC (64380-873-71) 64380-873-91 10 CUP, UNIT-DOSE in 1 TRAY (64380-873-91) / 15 mL in 1 CUP, UNIT-DOSE

Ingredients (1)

POTASSIUM CHLORIDE (20 meq/15mL)

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "58d1944f-cc5c-4cac-b559-f77fdb5c4f0c", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["fb859382-662c-49c3-bc62-98e9f30fd4ae"], "manufacturer_name": ["Strides Pharma Science Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CUP, UNIT-DOSE in 1 TRAY (64380-873-59)  / 30 mL in 1 CUP, UNIT-DOSE", "package_ndc": "64380-873-59", "marketing_start_date": "20250806"}, {"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (64380-873-71)", "package_ndc": "64380-873-71", "marketing_start_date": "20250806"}, {"sample": false, "description": "10 CUP, UNIT-DOSE in 1 TRAY (64380-873-91)  / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "64380-873-91", "marketing_start_date": "20250806"}], "brand_name": "Potassium Chloride", "product_id": "64380-873_58d1944f-cc5c-4cac-b559-f77fdb5c4f0c", "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": "64380-873", "generic_name": "Potassium Chloride", "labeler_name": "Strides Pharma Science Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA211665", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}