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Rx Act all day allergy relief - 37808-458-39 - (Cetirizine Hydrochloride)

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Drug Information of Rx Act all day allergy relief

Product NDC: 37808-458
Proprietary Name: Rx Act all day allergy relief
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Rx Act all day allergy relief

Product NDC: 37808-458
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20080131

Package Information of Rx Act all day allergy relief

Package NDC: 37808-458-39
Package Description: 1 BOTTLE in 1 CARTON (37808-458-39) > 30 TABLET in 1 BOTTLE

NDC Information of Rx Act all day allergy relief

NDC Code 37808-458-39
Proprietary Name Rx Act all day allergy relief
Package Description 1 BOTTLE in 1 CARTON (37808-458-39) > 30 TABLET in 1 BOTTLE
Product NDC 37808-458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080131
Marketing Category Name ANDA
Labeler Name H E B
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rx Act all day allergy relief


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