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"61919-886-30" National Drug Code (NDC)
Meclizine Hydrochloride 30 TABLET in 1 BOTTLE (61919-886-30)
(Direct_Rx)
NDC Code
61919-886-30
Package Description
30 TABLET in 1 BOTTLE (61919-886-30)
Product NDC
61919-886
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Meclizine Hydrochloride
Non-Proprietary Name
Meclizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20190801
Marketing Category Name
ANDA
Application Number
ANDA040659
Manufacturer
Direct_Rx
Substance Name
MECLIZINE HYDROCHLORIDE
Strength
12.5
Strength Unit
mg/1
Pharmacy Classes
Antiemetic [EPC], Emesis Suppression [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-886-30