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"68001-235-03" National Drug Code (NDC)

Potassium Chloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-03)
(BluePoint Laboratories)

NDC Code68001-235-03
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-03)
Product NDC68001-235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140225
End Marketing Date20221130
Marketing Category NameANDA
Application NumberANDA076368
ManufacturerBluePoint Laboratories
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-235-03





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