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"70518-2279-0" National Drug Code (NDC)
Hydroxyzine Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2279-0)
(REMEDYREPACK INC.)
NDC Code
70518-2279-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2279-0)
Product NDC
70518-2279
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Hydroxyzine Hydrochloride
Non-Proprietary Name
Hydroxyzine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20190824
Marketing Category Name
ANDA
Application Number
ANDA088618
Manufacturer
REMEDYREPACK INC.
Substance Name
HYDROXYZINE DIHYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2279-0