Sodium Nitrite (Hope Pharmaceuticals)
Welcome to the PulseAid listing for the Sodium Nitrite drug offered from Hope Pharmaceuticals. 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: | Hope Pharmaceuticals |
NON-PROPRIETARY NAME: | Sodium Nitrite |
SUBSTANCE NAME: | SODIUM NITRITE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2012-02-14 |
END MARKETING DATE: | 0000-00-00 |
Sodium Nitrite HUMAN PRESCRIPTION DRUG Details:
Item Description | Sodium Nitrite from Hope Pharmaceuticals |
LABELER NAME: | Hope Pharmaceuticals |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 30(mg/mL) |
START MARKETING DATE: | 2012-02-14 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60267-311_95ff0775-a09d-4cdb-83d9-4f86d9ac45d9 |
PRODUCT NDC: | 60267-311 |
APPLICATION NUMBER: | NDA203922 |
Other SODIUM NITRITE Pharmaceutical Manufacturers / Labelers: