Papaverine Hydrochloride (American Regent, Inc.)
Welcome to the PulseAid listing for the Papaverine Hydrochloride drug offered from American Regent, Inc.. 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: | American Regent, Inc. |
| NON-PROPRIETARY NAME: | Papaverine Hydrochloride |
| SUBSTANCE NAME: | PAPAVERINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 1995-09-01 |
| END MARKETING DATE: | 0000-00-00 |
Papaverine Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Papaverine Hydrochloride from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 30(mg/mL) |
| START MARKETING DATE: | 1995-09-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-4002_ac8f5e38-3e5b-4879-8d91-125a781e364f |
| PRODUCT NDC: | 0517-4002 |
| APPLICATION NUMBER: | |
Other PAPAVERINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
