Home > National Drug Code (NDC) > Loratadine Allergy Relief

Loratadine Allergy Relief - 51660-526-01 - (Loratadine)

Alphabetical Index


Drug Information of Loratadine Allergy Relief

Product NDC: 51660-526
Proprietary Name: Loratadine Allergy Relief
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 Loratadine Allergy Relief

Product NDC: 51660-526
Labeler Name: Ohm Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076134
Marketing Category: ANDA
Start Marketing Date: 20030828

Package Information of Loratadine Allergy Relief

Package NDC: 51660-526-01
Package Description: 100 TABLET in 1 BOTTLE (51660-526-01)

NDC Information of Loratadine Allergy Relief

NDC Code 51660-526-01
Proprietary Name Loratadine Allergy Relief
Package Description 100 TABLET in 1 BOTTLE (51660-526-01)
Product NDC 51660-526
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030828
Marketing Category Name ANDA
Labeler Name Ohm Laboratories Inc.
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine Allergy Relief


General Information