"24979-231-03" National Drug Code (NDC)

Potassium Chloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)
(TWi Pharmaceuticals, Inc.)

NDC Code24979-231-03
Package Description1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-231-03)
Product NDC24979-231
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePotassium Chloride
Proprietary Name SuffixExtended-release
Non-Proprietary NamePotassium Chloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230410
Marketing Category NameANDA
Application NumberANDA209688
ManufacturerTWi Pharmaceuticals, Inc.
Substance NamePOTASSIUM CHLORIDE
Strength750
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]

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