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"68788-8435-3" National Drug Code (NDC)
Cetirizine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (68788-8435-3)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-8435-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (68788-8435-3)
Product NDC
68788-8435
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride
Non-Proprietary Name
Cetirizine Hydrochloride Tablets
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230427
Marketing Category Name
ANDA
Application Number
ANDA078343
Manufacturer
Preferred 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/68788-8435-3