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TERBUTALINE SULFATE - 43063-059-08 - (TERBUTALINE SULFATE)

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Drug Information of TERBUTALINE SULFATE

Product NDC: 43063-059
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: 43063-059
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075877
Marketing Category: ANDA
Start Marketing Date: 20010626

Package Information of TERBUTALINE SULFATE

Package NDC: 43063-059-08
Package Description: 8 TABLET in 1 BOTTLE, PLASTIC (43063-059-08)

NDC Information of TERBUTALINE SULFATE

NDC Code 43063-059-08
Proprietary Name TERBUTALINE SULFATE
Package Description 8 TABLET in 1 BOTTLE, PLASTIC (43063-059-08)
Product NDC 43063-059
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 PD-Rx Pharmaceuticals, Inc.
Substance Name TERBUTALINE SULFATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of TERBUTALINE SULFATE


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