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"59651-429-99" National Drug Code (NDC)
Potassium Chloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-429-99)
(Aurobindo Pharma Limited)
NDC Code
59651-429-99
Package Description
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-429-99)
Product NDC
59651-429
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Potassium Chloride
Non-Proprietary Name
Potassium Chloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20210331
Marketing Category Name
ANDA
Application Number
ANDA214728
Manufacturer
Aurobindo Pharma Limited
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/59651-429-99