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