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"70518-3815-0" National Drug Code (NDC)
Meclizine Hydrochloride 21 TABLET in 1 BOTTLE, PLASTIC (70518-3815-0)
(REMEDYREPACK INC.)
NDC Code
70518-3815-0
Package Description
21 TABLET in 1 BOTTLE, PLASTIC (70518-3815-0)
Product NDC
70518-3815
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Meclizine Hydrochloride
Non-Proprietary Name
Meclizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230802
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA010721
Manufacturer
REMEDYREPACK INC.
Substance Name
MECLIZINE HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Antiemetic [EPC], Emesis Suppression [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3815-0