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"69097-812-12" National Drug Code (NDC)
Gabapentin 500 TABLET in 1 BOTTLE (69097-812-12)
(Cipla USA Inc.)
NDC Code
69097-812-12
Package Description
500 TABLET in 1 BOTTLE (69097-812-12)
Product NDC
69097-812
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160722
Marketing Category Name
ANDA
Application Number
ANDA202764
Manufacturer
Cipla USA Inc.
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/69097-812-12