Terbutaline Sulfate (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Terbutaline Sulfate drug offered from APP Pharmaceuticals, LLC. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | APP Pharmaceuticals, LLC |
| NON-PROPRIETARY NAME: | TERBUTALINE SULFATE |
| SUBSTANCE NAME: | TERBUTALINE SULFATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | SUBCUTANEOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2011-03-10 |
| END MARKETING DATE: | 0000-00-00 |
Terbutaline Sulfate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Terbutaline Sulfate from APP Pharmaceuticals, LLC |
| LABELER NAME: | APP Pharmaceuticals, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(mg/mL) |
| START MARKETING DATE: | 2011-03-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-665_be203fdb-578c-49a1-8a77-b15b80377d75 |
| PRODUCT NDC: | 63323-665 |
| APPLICATION NUMBER: | ANDA076887 |
Other TERBUTALINE SULFATE Pharmaceutical Manufacturers / Labelers:
