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TERBUTALINE SULFATE - 0115-2622-02 - (TERBUTALINE SULFATE)

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Drug Information of TERBUTALINE SULFATE

Product NDC: 0115-2622
Proprietary Name: TERBUTALINE SULFATE
Non Proprietary Name: TERBUTALINE SULFATE
Active Ingredient(s): 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: 0115-2622
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075877
Marketing Category: ANDA
Start Marketing Date: 20010626

Package Information of TERBUTALINE SULFATE

Package NDC: 0115-2622-02
Package Description: 500 TABLET in 1 BOTTLE (0115-2622-02)

NDC Information of TERBUTALINE SULFATE

NDC Code 0115-2622-02
Proprietary Name TERBUTALINE SULFATE
Package Description 500 TABLET in 1 BOTTLE (0115-2622-02)
Product NDC 0115-2622
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TERBUTALINE SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010626
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name TERBUTALINE SULFATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of TERBUTALINE SULFATE


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