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"70518-0669-0" National Drug Code (NDC)
Metoclopramide 30 TABLET in 1 BLISTER PACK (70518-0669-0)
(REMEDYREPACK INC.)
NDC Code
70518-0669-0
Package Description
30 TABLET in 1 BLISTER PACK (70518-0669-0)
Product NDC
70518-0669
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Metoclopramide
Non-Proprietary Name
Metoclopramide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190814
Marketing Category Name
ANDA
Application Number
ANDA070184
Manufacturer
REMEDYREPACK 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/70518-0669-0