Home > National Drug Code (NDC) > Childrens Non-Drowsy

Childrens Non-Drowsy - 21130-787-29 - (Loratadine)

Alphabetical Index


Drug Information of Childrens Non-Drowsy

Product NDC: 21130-787
Proprietary Name: Childrens Non-Drowsy
Non Proprietary Name: Loratadine
Active Ingredient(s): 5    mg/5mL & nbsp;   Loratadine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Non-Drowsy

Product NDC: 21130-787
Labeler Name: Safeway Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076805
Marketing Category: ANDA
Start Marketing Date: 20040820

Package Information of Childrens Non-Drowsy

Package NDC: 21130-787-29
Package Description: 1 BOTTLE in 1 CARTON (21130-787-29) > 120 mL in 1 BOTTLE

NDC Information of Childrens Non-Drowsy

NDC Code 21130-787-29
Proprietary Name Childrens Non-Drowsy
Package Description 1 BOTTLE in 1 CARTON (21130-787-29) > 120 mL in 1 BOTTLE
Product NDC 21130-787
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Loratadine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20040820
Marketing Category Name ANDA
Labeler Name Safeway Inc.
Substance Name LORATADINE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Childrens Non-Drowsy


General Information