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"53002-1035-3" National Drug Code (NDC)

Potassium Chloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1035-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1035-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1035-3)
Product NDC53002-1035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040818
Marketing Category NameANDA
Application NumberANDA076368
ManufacturerRPK 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-1035-3





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