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"60687-708-09" National Drug Code (NDC)
Potassium Chloride 80 BLISTER PACK in 1 CARTON (60687-708-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-708-11)
(American Health Packaging)
NDC Code
60687-708-09
Package Description
80 BLISTER PACK in 1 CARTON (60687-708-09) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-708-11)
Product NDC
60687-708
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Potassium Chloride
Non-Proprietary Name
Potassium Chloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20230227
End Marketing Date
20241031
Marketing Category Name
ANDA
Application Number
ANDA210733
Manufacturer
American Health Packaging
Substance Name
POTASSIUM CHLORIDE
Strength
750
Strength Unit
mg/1
Pharmacy Classes
Increased 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/60687-708-09