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"10135-762-01" National Drug Code (NDC)
Cetirizine Hydrochloride 100 TABLET in 1 BOTTLE (10135-762-01)
(Marlex Pharmaceuticals, Inc)
NDC Code
10135-762-01
Package Description
100 TABLET in 1 BOTTLE (10135-762-01)
Product NDC
10135-762
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20221001
Marketing Category Name
ANDA
Application Number
ANDA077498
Manufacturer
Marlex Pharmaceuticals, Inc
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/10135-762-01