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"70692-139-14" National Drug Code (NDC)
Cetirizine Hydrochloride 14 TABLET in 1 BOTTLE (70692-139-14)
(Strive Pharmaceuticals Inc)
NDC Code
70692-139-14
Package Description
14 TABLET in 1 BOTTLE (70692-139-14)
Product NDC
70692-139
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20200701
Marketing Category Name
ANDA
Application Number
ANDA209274
Manufacturer
Strive 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/70692-139-14