Package 0121-4948-40

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0121-4948-40
Digits Only 0121494840
Product NDC 0121-4948
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)

Marketing

Marketing Status
Marketed Since 2023-03-27
Brand potassium chloride
Generic potassium chloride
Sample Package No

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"}