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"52125-984-19" National Drug Code (NDC)
Gabapentin 90 TABLET in 1 BOTTLE (52125-984-19)
(REMEDYREPACK INC.)
NDC Code
52125-984-19
Package Description
90 TABLET in 1 BOTTLE (52125-984-19)
Product NDC
52125-984
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160408
End Marketing Date
20170526
Marketing Category Name
ANDA
Application Number
ANDA202764
Manufacturer
REMEDYREPACK INC.
Substance Name
GABAPENTIN
Strength
800
Strength Unit
mg/1
Pharmacy Classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-984-19