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"55111-351-74" National Drug Code (NDC)
Cetirizine Hydrochloride 2 BLISTER PACK in 1 CARTON (55111-351-74) > 7 TABLET, FILM COATED in 1 BLISTER PACK
(Dr.Reddy's Laboratories Limited)
NDC Code
55111-351-74
Package Description
2 BLISTER PACK in 1 CARTON (55111-351-74) > 7 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
55111-351
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20080115
Marketing Category Name
ANDA
Application Number
ANDA078343
Manufacturer
Dr.Reddy's Laboratories Limited
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
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/55111-351-74