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"70518-2317-1" National Drug Code (NDC)
Escitalopram 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)
(REMEDYREPACK INC.)
NDC Code
70518-2317-1
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)
Product NDC
70518-2317
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Escitalopram
Non-Proprietary Name
Escitalopram
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190909
Marketing Category Name
ANDA
Application Number
ANDA078032
Manufacturer
REMEDYREPACK INC.
Substance Name
ESCITALOPRAM OXALATE
Strength
20
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/70518-2317-1