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Terbutaline Sulfate - 55390-101-10 - (Terbutaline Sulfate)

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Drug Information of Terbutaline Sulfate

Product NDC: 55390-101
Proprietary Name: Terbutaline Sulfate
Non Proprietary Name: Terbutaline Sulfate
Active Ingredient(s): 1    mg/mL & nbsp;   Terbutaline Sulfate
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Terbutaline Sulfate

Product NDC: 55390-101
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076770
Marketing Category: ANDA
Start Marketing Date: 20040428

Package Information of Terbutaline Sulfate

Package NDC: 55390-101-10
Package Description: 10 VIAL in 1 BOX (55390-101-10) > 1 mL in 1 VIAL

NDC Information of Terbutaline Sulfate

NDC Code 55390-101-10
Proprietary Name Terbutaline Sulfate
Package Description 10 VIAL in 1 BOX (55390-101-10) > 1 mL in 1 VIAL
Product NDC 55390-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbutaline Sulfate
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20040428
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name TERBUTALINE SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Terbutaline Sulfate


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