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"68001-566-03" National Drug Code (NDC)
Potassium Chloride Extended-release 500 TABLET in 1 BOTTLE (68001-566-03)
(Bluepoint Laboratories)
NDC Code
68001-566-03
Package Description
500 TABLET in 1 BOTTLE (68001-566-03)
Product NDC
68001-566
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Potassium Chloride Extended-release
Non-Proprietary Name
Potassium Chloride Extended-release
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20210130
Marketing Category Name
ANDA
Application Number
ANDA214452
Manufacturer
Bluepoint Laboratories
Substance Name
POTASSIUM CHLORIDE
Strength
750
Strength Unit
mg/1
Pharmacy 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]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-566-03