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Terbutaline Sulfate
Terbutaline Sulfate - 68084-257-21 - (Terbutaline Sulfate)
Drug Information of Terbutaline Sulfate
| Product NDC: | 68084-257 |
| 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: | 68084-257 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077152 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080312 |
Package Information of Terbutaline Sulfate
| Package NDC: | 68084-257-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-257-21) > 10 TABLET in 1 BLISTER PACK (68084-257-11) (68084-257-11) |
NDC Information of Terbutaline Sulfate
| NDC Code | 68084-257-21 |
| Proprietary Name | Terbutaline Sulfate |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-257-21) > 10 TABLET in 1 BLISTER PACK (68084-257-11) (68084-257-11) |
| Product NDC | 68084-257 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terbutaline Sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080312 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | TERBUTALINE SULFATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
