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Loratadine and Pseudoephedrine - 63629-1330-2 - (loratadine and pseudoephedrine)

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Drug Information of Loratadine and Pseudoephedrine

Product NDC: 63629-1330
Proprietary Name: Loratadine and Pseudoephedrine
Non Proprietary Name: loratadine and pseudoephedrine
Active Ingredient(s): 10; 240    mg/1; mg/1 & nbsp;   loratadine and pseudoephedrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine and Pseudoephedrine

Product NDC: 63629-1330
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076557
Marketing Category: ANDA
Start Marketing Date: 20041117

Package Information of Loratadine and Pseudoephedrine

Package NDC: 63629-1330-2
Package Description: 5 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1330-2)

NDC Information of Loratadine and Pseudoephedrine

NDC Code 63629-1330-2
Proprietary Name Loratadine and Pseudoephedrine
Package Description 5 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1330-2)
Product NDC 63629-1330
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name loratadine and pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20041117
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 10; 240
Strength Unit mg/1; mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Loratadine and Pseudoephedrine


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