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Terbutaline Sulfate - 0527-1318-10 - (Terbutaline Sulfate)

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Drug Information of Terbutaline Sulfate

Product NDC: 0527-1318
Proprietary Name: Terbutaline Sulfate
Non Proprietary Name: Terbutaline Sulfate
Active Ingredient(s): 2.5    mg/1 & nbsp;   Terbutaline Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Terbutaline Sulfate

Product NDC: 0527-1318
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077152
Marketing Category: ANDA
Start Marketing Date: 20050325

Package Information of Terbutaline Sulfate

Package NDC: 0527-1318-10
Package Description: 1000 TABLET in 1 BOTTLE (0527-1318-10)

NDC Information of Terbutaline Sulfate

NDC Code 0527-1318-10
Proprietary Name Terbutaline Sulfate
Package Description 1000 TABLET in 1 BOTTLE (0527-1318-10)
Product NDC 0527-1318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbutaline Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050325
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name TERBUTALINE SULFATE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Terbutaline Sulfate


General Information