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"71205-931-30" National Drug Code (NDC)
Gabapentin 30 TABLET in 1 BOTTLE (71205-931-30)
(Proficient Rx LP)
NDC Code
71205-931-30
Package Description
30 TABLET in 1 BOTTLE (71205-931-30)
Product NDC
71205-931
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160411
Marketing Category Name
ANDA
Application Number
ANDA205101
Manufacturer
Proficient Rx LP
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/71205-931-30