Loratadine - 21695-499-90 - (Loratadine)

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Drug Information of Loratadine

Product NDC: 21695-499
Proprietary Name: Loratadine
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

Product NDC: 21695-499
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100121

Package Information of Loratadine

Package NDC: 21695-499-90
Package Description: 90 TABLET in 1 BOTTLE (21695-499-90)

NDC Information of Loratadine

NDC Code 21695-499-90
Proprietary Name Loratadine
Package Description 90 TABLET in 1 BOTTLE (21695-499-90)
Product NDC 21695-499
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100121
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Rebel Distributors Corp
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Loratadine


General Information