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"70710-1221-1" National Drug Code (NDC)
Carbidopa 100 TABLET in 1 BOTTLE (70710-1221-1)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
70710-1221-1
Package Description
100 TABLET in 1 BOTTLE (70710-1221-1)
Product NDC
70710-1221
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Carbidopa
Non-Proprietary Name
Carbidopa
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180906
Marketing Category Name
ANDA
Application Number
ANDA209910
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
CARBIDOPA
Strength
25
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70710-1221-1