allergy - 0904-5728-89 - (Loratadine)

Alphabetical Index


Drug Information of allergy

Product NDC: 0904-5728
Proprietary Name: allergy
Non Proprietary Name: Loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of allergy

Product NDC: 0904-5728
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076301
Marketing Category: ANDA
Start Marketing Date: 20050221

Package Information of allergy

Package NDC: 0904-5728-89
Package Description: 1 BOTTLE in 1 CARTON (0904-5728-89) > 90 TABLET in 1 BOTTLE

NDC Information of allergy

NDC Code 0904-5728-89
Proprietary Name allergy
Package Description 1 BOTTLE in 1 CARTON (0904-5728-89) > 90 TABLET in 1 BOTTLE
Product NDC 0904-5728
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050221
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of allergy


General Information