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Loratadine D - 63629-4790-1 - (Loratadine, Pseudoephedrine)

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Drug Information of Loratadine D

Product NDC: 63629-4790
Proprietary Name: Loratadine D
Non Proprietary Name: Loratadine, Pseudoephedrine
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Loratadine, Pseudoephedrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Loratadine D

Product NDC: 63629-4790
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076050
Marketing Category: ANDA
Start Marketing Date: 20120119

Package Information of Loratadine D

Package NDC: 63629-4790-1
Package Description: 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4790-1)

NDC Information of Loratadine D

NDC Code 63629-4790-1
Proprietary Name Loratadine D
Package Description 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4790-1)
Product NDC 63629-4790
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Loratadine, Pseudoephedrine
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120119
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name LORATADINE; PSEUDOEPHEDRINE SULFATE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Loratadine D


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