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"61919-677-30" National Drug Code (NDC)
Gabapentin 30 TABLET in 1 BOTTLE (61919-677-30)
(DIRECTRX)
NDC Code
61919-677-30
Package Description
30 TABLET in 1 BOTTLE (61919-677-30)
Product NDC
61919-677
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190411
Marketing Category Name
ANDA
Application Number
ANDA077662
Manufacturer
DIRECTRX
Substance Name
GABAPENTIN
Strength
600
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/61919-677-30