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"68210-0119-3" National Drug Code (NDC)
Cabinet Allergy Relief 1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
(Spirit Pharmaceutical LLC)
NDC Code
68210-0119-3
Package Description
1 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC
68210-0119
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cabinet Allergy Relief
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20191025
Marketing Category Name
ANDA
Application Number
ANDA209274
Manufacturer
Spirit Pharmaceutical LLC
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/68210-0119-3