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"68071-4332-2" National Drug Code (NDC)
Escitalopram 20 TABLET, FILM COATED in 1 BOTTLE (68071-4332-2)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-4332-2
Package Description
20 TABLET, FILM COATED in 1 BOTTLE (68071-4332-2)
Product NDC
68071-4332
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Escitalopram
Non-Proprietary Name
Escitalopram
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120314
Marketing Category Name
ANDA
Application Number
ANDA076765
Manufacturer
NuCare Pharmaceuticals,Inc.
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/68071-4332-2