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"68001-196-03" National Drug Code (NDC)
Escitalopram 500 TABLET, FILM COATED in 1 BOTTLE (68001-196-03)
(BluePoint Laboratories)
NDC Code
68001-196-03
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (68001-196-03)
Product NDC
68001-196
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Escitalopram
Non-Proprietary Name
Escitalopram Oxalate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140206
End Marketing Date
20240131
Marketing Category Name
ANDA
Application Number
ANDA202280
Manufacturer
BluePoint Laboratories
Substance Name
ESCITALOPRAM OXALATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68001-196-03