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"53002-1039-2" National Drug Code (NDC)

Potassium Chloride 20 TABLET, EXTENDED RELEASE in 1 BOTTLE, DROPPER (53002-1039-2)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1039-2
Package Description20 TABLET, EXTENDED RELEASE in 1 BOTTLE, DROPPER (53002-1039-2)
Product NDC53002-1039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20181119
Marketing Category NameANDA
Application NumberANDA210733
ManufacturerRPK Pharmaceuticals, Inc.
Substance NamePOTASSIUM CHLORIDE
Strength600
Strength Unitmg/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/53002-1039-2





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