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"68682-200-25" National Drug Code (NDC)
Carbidopa 100 TABLET in 1 BOTTLE (68682-200-25)
(Oceanside Pharmaceuticals)
NDC Code
68682-200-25
Package Description
100 TABLET in 1 BOTTLE (68682-200-25)
Product NDC
68682-200
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carbidopa
Non-Proprietary Name
Carbidopa Tablets
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140404
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA017830
Manufacturer
Oceanside Pharmaceuticals
Substance Name
CARBIDOPA
Strength
25
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68682-200-25