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"68001-235-08" National Drug Code (NDC)
Potassium Chloride 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-08)
(BluePoint Laboratories)
NDC Code
68001-235-08
Package Description
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-08)
Product NDC
68001-235
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
20140225
End Marketing Date
20221130
Marketing Category Name
ANDA
Application Number
ANDA076368
Manufacturer
BluePoint Laboratories
Substance Name
POTASSIUM CHLORIDE
Strength
20
Strength Unit
meq/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/68001-235-08