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Terbutaline Sulfate
Terbutaline Sulfate - 0143-9746-10 - (Terbutaline Sulfate)
Drug Information of Terbutaline Sulfate
| Product NDC: | 0143-9746 |
| 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: | 0143-9746 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078630 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090520 |
Package Information of Terbutaline Sulfate
| Package NDC: | 0143-9746-10 |
| Package Description: | 10 VIAL in 1 CARTON (0143-9746-10) > 1 mL in 1 VIAL (0143-9746-01) |
NDC Information of Terbutaline Sulfate
| NDC Code | 0143-9746-10 |
| Proprietary Name | Terbutaline Sulfate |
| Package Description | 10 VIAL in 1 CARTON (0143-9746-10) > 1 mL in 1 VIAL (0143-9746-01) |
| Product NDC | 0143-9746 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terbutaline Sulfate |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090520 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | TERBUTALINE SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
