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"11822-7053-8" National Drug Code (NDC)
Cetirizine Hydrochloride 1 BOTTLE in 1 CARTON (11822-7053-8) > 30 TABLET, FILM COATED in 1 BOTTLE
(Rite Aid Corporation)
NDC Code
11822-7053-8
Package Description
1 BOTTLE in 1 CARTON (11822-7053-8) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC
11822-7053
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
20170525
End Marketing Date
20210430
Marketing Category Name
ANDA
Application Number
ANDA078317
Manufacturer
Rite Aid Corporation
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/11822-7053-8