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"0093-2203-05" National Drug Code (NDC)
Metoclopramide 500 TABLET in 1 BOTTLE (0093-2203-05)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-2203-05
Package Description
500 TABLET in 1 BOTTLE (0093-2203-05)
Product NDC
0093-2203
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Metoclopramide
Non-Proprietary Name
Metoclopramide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
19900930
Marketing Category Name
ANDA
Application Number
ANDA070184
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
METOCLOPRAMIDE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-2203-05