"43386-917-05" National Drug Code (NDC)

Potassium Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05)
(Lupin Pharmaceuticals,Inc.)

NDC Code43386-917-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05)
Product NDC43386-917
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160121
Marketing Category NameANDA
Application NumberANDA206347
ManufacturerLupin Pharmaceuticals,Inc.
Substance NamePOTASSIUM CHLORIDE
Strength20
Strength Unitmeq/1
Pharmacy ClassesIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]

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