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"76420-837-05" National Drug Code (NDC)
Gabapentin 500 TABLET in 1 BOTTLE (76420-837-05)
(Asclemed USA, Inc.)
NDC Code
76420-837-05
Package Description
500 TABLET in 1 BOTTLE (76420-837-05)
Product NDC
76420-837
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20211001
Marketing Category Name
ANDA
Application Number
ANDA214957
Manufacturer
Asclemed USA, Inc.
Substance Name
GABAPENTIN
Strength
800
Strength Unit
mg/1
Pharmacy Classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/76420-837-05