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Terbutaline Sulfate - 53808-0312-1 - (TERBUTALINE SULFATE)

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Drug Information of Terbutaline Sulfate

Product NDC: 53808-0312
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: 53808-0312
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077152
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Terbutaline Sulfate

Package NDC: 53808-0312-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0312-1)

NDC Information of Terbutaline Sulfate

NDC Code 53808-0312-1
Proprietary Name Terbutaline Sulfate
Package Description 30 TABLET in 1 BLISTER PACK (53808-0312-1)
Product NDC 53808-0312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TERBUTALINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name TERBUTALINE SULFATE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Terbutaline Sulfate


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