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"43386-917-05" National Drug Code (NDC)
Potassium Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05)
(Lupin Pharmaceuticals,Inc.)
NDC Code
43386-917-05
Package Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05)
Product NDC
43386-917
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
20160121
Marketing Category Name
ANDA
Application Number
ANDA206347
Manufacturer
Lupin Pharmaceuticals,Inc.
Substance Name
POTASSIUM CHLORIDE
Strength
20
Strength Unit
meq/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/43386-917-05