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"37808-458-66" National Drug Code (NDC)
Rx Act All Day Allergy Relief 1 BLISTER PACK in 1 CARTON (37808-458-66) > 14 TABLET in 1 BLISTER PACK
(H E B)
NDC Code
37808-458-66
Package Description
1 BLISTER PACK in 1 CARTON (37808-458-66) > 14 TABLET in 1 BLISTER PACK
Product NDC
37808-458
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Rx Act All Day Allergy Relief
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20080131
Marketing Category Name
ANDA
Application Number
ANDA078336
Manufacturer
H E B
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-458-66