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"69844-091-03" National Drug Code (NDC)
Gabapentin 500 TABLET in 1 BOTTLE (69844-091-03)
(Graviti Pharmaceuticals Private Limited)
NDC Code
69844-091-03
Package Description
500 TABLET in 1 BOTTLE (69844-091-03)
Product NDC
69844-091
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230719
Marketing Category Name
ANDA
Application Number
ANDA217995
Manufacturer
Graviti Pharmaceuticals Private Limited
Substance Name
GABAPENTIN
Strength
600
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/69844-091-03