Norepinephrine Bitartrate (Teva Parenteral Medicines, Inc.)
Welcome to the PulseAid listing for the Norepinephrine Bitartrate drug offered from Teva Parenteral Medicines, Inc.. This Catecholamine [EPC],Catecholamines [Chemical/Ingredient] 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: | Teva Parenteral Medicines, Inc. |
| NON-PROPRIETARY NAME: | Norepinephrine Bitartrate |
| SUBSTANCE NAME: | NOREPINEPHRINE BITARTRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2003-04-01 |
| END MARKETING DATE: | 0000-00-00 |
Norepinephrine Bitartrate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Norepinephrine Bitartrate from Teva Parenteral Medicines, Inc. |
| LABELER NAME: | Teva Parenteral Medicines, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 1(mg/mL) |
| START MARKETING DATE: | 2003-04-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0703-1153_b7afe372-f231-4d5b-8c1d-1d76a85b4251 |
| PRODUCT NDC: | 0703-1153 |
| APPLICATION NUMBER: | ANDA040455 |
Other NOREPINEPHRINE BITARTRATE Pharmaceutical Manufacturers / Labelers:
