Package 0121-0948-16
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
0121-0948-16
Digits Only
0121094816
Product NDC
0121-0948
Description
473 mL in 1 BOTTLE (0121-0948-16)
Marketing
Marketing Status
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": "473 mL in 1 BOTTLE (0121-0948-16)", "package_ndc": "0121-0948-16", "marketing_start_date": "20230327"}], "brand_name": "Potassium Chloride", "product_id": "0121-0948_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": "0121-0948", "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"}