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"49349-088-02" National Drug Code (NDC)
Cetirizine Hydrochloride 30 TABLET in 1 BLISTER PACK (49349-088-02)
(REMEDYREPACK INC.)
NDC Code
49349-088-02
Package Description
30 TABLET in 1 BLISTER PACK (49349-088-02)
Product NDC
49349-088
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20101123
Marketing Category Name
ANDA
Application Number
ANDA078317
Manufacturer
REMEDYREPACK INC.
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-088-02