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All day Allergy d - 0904-5831-12 - (Cetirizine HCl, Pseudoephedrine HCl)

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Drug Information of All day Allergy d

Product NDC: 0904-5831
Proprietary Name: All day Allergy d
Non Proprietary Name: Cetirizine HCl, Pseudoephedrine HCl
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Cetirizine HCl, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of All day Allergy d

Product NDC: 0904-5831
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077170
Marketing Category: ANDA
Start Marketing Date: 20080506

Package Information of All day Allergy d

Package NDC: 0904-5831-12
Package Description: 2 BLISTER PACK in 1 CARTON (0904-5831-12) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of All day Allergy d

NDC Code 0904-5831-12
Proprietary Name All day Allergy d
Package Description 2 BLISTER PACK in 1 CARTON (0904-5831-12) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 0904-5831
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl, Pseudoephedrine HCl
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080506
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of All day Allergy d


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