Home > National Drug Code (NDC) > ALAVERT ALLERGY

ALAVERT ALLERGY - 0573-2620-19 - (loratadine)

Alphabetical Index


Drug Information of ALAVERT ALLERGY

Product NDC: 0573-2620
Proprietary Name: ALAVERT ALLERGY
Non Proprietary Name: loratadine
Active Ingredient(s): 10    mg/1 & nbsp;   loratadine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of ALAVERT ALLERGY

Product NDC: 0573-2620
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021375
Marketing Category: NDA
Start Marketing Date: 20021219

Package Information of ALAVERT ALLERGY

Package NDC: 0573-2620-19
Package Description: 3 BLISTER PACK in 1 CARTON (0573-2620-19) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of ALAVERT ALLERGY

NDC Code 0573-2620-19
Proprietary Name ALAVERT ALLERGY
Package Description 3 BLISTER PACK in 1 CARTON (0573-2620-19) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 0573-2620
Product Type Name HUMAN OTC DRUG
Non Proprietary Name loratadine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20021219
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name LORATADINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ALAVERT ALLERGY


General Information