The NDC Code 0121-0466-16 is assigned to a package of 473 ml in 1 bottle of Potassium Chloride, labeled by Pharmaceutical Associates, Inc.. The product's dosage form is and is administered via form.
The National Average Drug Acquisition Cost (NADAC) wholesale price per unit for NDC 0121-0466-16 is $0.82656 and is up-to-date as of 05-23-2018.
||473 mL in 1 BOTTLE
||Potassium Chloride What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
||This medication is a mineral supplement used to treat or prevent low amounts of potassium in the blood. A normal level of potassium in the blood is important. Potassium helps your cells, kidneys, heart, muscles, and nerves work properly. Most people get enough potassium by eating a well-balanced diet. Some conditions that can lower your body's potassium level include severe prolonged diarrhea and vomiting, hormone problems such as hyperaldosteronism, or treatment with "water pills"/diuretics.
|11-Digit NDC Billing Format
||00121046616 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
||ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
|RxNorm Crosswalk||314182 - RxCUI What is RxNorm?|
The RxNorm crosswalk provides a normalized naming system for generic and branded drugs by assigning unique concept identifiers (RxCUI) to each NDC.
Pharmaceutical Associates, Inc.
||No Sample Package?
This field Indicates whether this package is a sample packaging or not.
|Start Marketing Date
||10-01-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
|Listing Expiration Date
||12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
||I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Code Structure
- 0121 - Pharmaceutical Associates, Inc.
- 0121-0466 - Potassium Chloride
0121-0466-16 - 473 mL in 1 BOTTLE
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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