potassium chloride

Generic: potassium chloride oral

Labeler: saptalis pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride
Generic Name potassium chloride oral
Labeler saptalis pharmaceuticals, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

potassium chloride 1.5 g/15mL

Manufacturer
Saptalis Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 71656-021
Product ID 71656-021_4872fd4b-ae1d-9c4c-e063-6294a90a7fc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211648
Listing Expiration 2027-12-31
Marketing Start 2023-10-05

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 71656021
Hyphenated Format 71656-021

Supplemental Identifiers

RxCUI
312515 314182
UPC
0371656021160
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 oral (source: ndc)
Application Number ANDA211648 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/15mL
source: ndc
Packaging
  • 10 TRAY in 1 CASE (71656-021-01) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)
  • 10 TRAY in 1 CASE (71656-021-02) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)
  • 473 mL in 1 BOTTLE (71656-021-16)
  • 5 TRAY in 1 CASE (71656-021-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)
  • 5 TRAY in 1 CASE (71656-021-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)
source: ndc

Packages (5)

71656-021-01 10 TRAY in 1 CASE (71656-021-01) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15) 71656-021-02 10 TRAY in 1 CASE (71656-021-02) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30) 71656-021-16 473 mL in 1 BOTTLE (71656-021-16) 71656-021-50 5 TRAY in 1 CASE (71656-021-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15) 71656-021-51 5 TRAY in 1 CASE (71656-021-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)

Ingredients (1)

potassium chloride (1.5 g/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": "4872fd4b-ae1d-9c4c-e063-6294a90a7fc6", "openfda": {"upc": ["0371656021160"], "unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["483f338e-a164-4c1f-a34e-fef3312cb7ec"], "manufacturer_name": ["Saptalis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (71656-021-01)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)", "package_ndc": "71656-021-01", "marketing_start_date": "20231005"}, {"sample": false, "description": "10 TRAY in 1 CASE (71656-021-02)  / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)", "package_ndc": "71656-021-02", "marketing_start_date": "20231005"}, {"sample": false, "description": "473 mL in 1 BOTTLE (71656-021-16)", "package_ndc": "71656-021-16", "marketing_start_date": "20231005"}, {"sample": false, "description": "5 TRAY in 1 CASE (71656-021-50)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15)", "package_ndc": "71656-021-50", "marketing_start_date": "20231005"}, {"sample": false, "description": "5 TRAY in 1 CASE (71656-021-51)  / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30)", "package_ndc": "71656-021-51", "marketing_start_date": "20231005"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "71656-021_4872fd4b-ae1d-9c4c-e063-6294a90a7fc6", "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": "71656-021", "generic_name": "POTASSIUM CHLORIDE ORAL", "labeler_name": "Saptalis Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1.5 g/15mL"}], "application_number": "ANDA211648", "marketing_category": "ANDA", "marketing_start_date": "20231005", "listing_expiration_date": "20271231"}