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allergy and congestion relief - 24385-351-22 - (Pseudoephedrine sulfate, Loratadine)

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Drug Information of allergy and congestion relief

Product NDC: 24385-351
Proprietary Name: allergy and congestion relief
Non Proprietary Name: Pseudoephedrine sulfate, Loratadine
Active Ingredient(s): 10; 240    mg/1; mg/1 & nbsp;   Pseudoephedrine sulfate, Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of allergy and congestion relief

Product NDC: 24385-351
Labeler Name: Amerisource Bergen
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075989
Marketing Category: ANDA
Start Marketing Date: 20101113

Package Information of allergy and congestion relief

Package NDC: 24385-351-22
Package Description: 3 BLISTER PACK in 1 CARTON (24385-351-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of allergy and congestion relief

NDC Code 24385-351-22
Proprietary Name allergy and congestion relief
Package Description 3 BLISTER PACK in 1 CARTON (24385-351-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 24385-351
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Pseudoephedrine sulfate, Loratadine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101113
Marketing Category Name ANDA
Labeler Name Amerisource Bergen
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 10; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of allergy and congestion relief


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