potassium chloride
Generic: potassium chloride
Labeler: pai holdings, llc dba pai pharmaDrug Facts
Product Profile
Brand Name
potassium chloride
Generic Name
potassium chloride
Labeler
pai holdings, llc dba pai pharma
Dosage Form
SOLUTION
Routes
Active Ingredients
potassium chloride 20 meq/15mL
Manufacturer
Identifiers & Regulatory
Product NDC
0121-4948
Product ID
0121-4948_f5027a39-0ab3-4d01-9f7a-3737c7e8e852
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210766
Listing Expiration
2026-12-31
Marketing Start
2023-03-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01214948
Hyphenated Format
0121-4948
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA210766 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 meq/15mL
Packaging
- 10 TRAY in 1 CASE (0121-4948-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
- 4 TRAY in 1 CASE (0121-4948-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
- 5 TRAY in 1 CASE (0121-4948-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
- 8 TRAY in 1 CASE (0121-4948-80) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
- 3 TRAY in 1 CASE (0121-4948-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
Packages (5)
0121-4948-00
10 TRAY in 1 CASE (0121-4948-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-40
4 TRAY in 1 CASE (0121-4948-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-50
5 TRAY in 1 CASE (0121-4948-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-80
8 TRAY in 1 CASE (0121-4948-80) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
0121-4948-94
3 TRAY in 1 CASE (0121-4948-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f5027a39-0ab3-4d01-9f7a-3737c7e8e852", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312515", "314182"], "spl_set_id": ["e848477f-b10d-4249-b322-b70cd6a062de"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-4948-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)", "package_ndc": "0121-4948-00", "marketing_start_date": "20230327"}, {"sample": false, "description": "4 TRAY in 1 CASE (0121-4948-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)", "package_ndc": "0121-4948-40", "marketing_start_date": "20230327"}, {"sample": false, "description": "5 TRAY in 1 CASE (0121-4948-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)", "package_ndc": "0121-4948-50", "marketing_start_date": "20230327"}, {"sample": false, "description": "8 TRAY in 1 CASE (0121-4948-80) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)", "package_ndc": "0121-4948-80", "marketing_start_date": "20230327"}, {"sample": false, "description": "3 TRAY in 1 CASE (0121-4948-94) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (0121-4948-15)", "package_ndc": "0121-4948-94", "marketing_start_date": "20230327"}], "brand_name": "Potassium Chloride", "product_id": "0121-4948_f5027a39-0ab3-4d01-9f7a-3737c7e8e852", "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": "0121-4948", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/15mL"}], "application_number": "ANDA210766", "marketing_category": "ANDA", "marketing_start_date": "20230327", "listing_expiration_date": "20261231"}