Home
>
National Drug Code (NDC)
>
Terbutaline Sulfate
Terbutaline Sulfate - 63323-665-01 - (TERBUTALINE SULFATE)
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 |
