Sunmark - 49348-849-34 - (Loratadine)

Alphabetical Index


Drug Information of Sunmark

Product NDC: 49348-849
Proprietary Name: Sunmark
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 Sunmark

Product NDC: 49348-849
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076805
Marketing Category: ANDA
Start Marketing Date: 20040820

Package Information of Sunmark

Package NDC: 49348-849-34
Package Description: 1 BOTTLE in 1 CARTON (49348-849-34) > 120 mL in 1 BOTTLE

NDC Information of Sunmark

NDC Code 49348-849-34
Proprietary Name Sunmark
Package Description 1 BOTTLE in 1 CARTON (49348-849-34) > 120 mL in 1 BOTTLE
Product NDC 49348-849
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 McKesson
Substance Name LORATADINE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Sunmark


General Information