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Terbutaline Sulfate - 63323-665-01 - (TERBUTALINE SULFATE)

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Drug Information of Terbutaline Sulfate

Product NDC: 63323-665
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Terbutaline Sulfate

Product NDC: 63323-665
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076887
Marketing Category: ANDA
Start Marketing Date: 20110310

Package Information of Terbutaline Sulfate

Package NDC: 63323-665-01
Package Description: 25 VIAL, SINGLE-USE in 1 TRAY (63323-665-01) > 1 mL in 1 VIAL, SINGLE-USE

NDC Information of Terbutaline Sulfate

NDC Code 63323-665-01
Proprietary Name Terbutaline Sulfate
Package Description 25 VIAL, SINGLE-USE in 1 TRAY (63323-665-01) > 1 mL in 1 VIAL, SINGLE-USE
Product NDC 63323-665
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TERBUTALINE SULFATE
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20110310
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name TERBUTALINE SULFATE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Terbutaline Sulfate


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