Thiamine (Fresenius Kabi USA, LLC)
Welcome to the PulseAid listing for the Thiamine drug offered from Fresenius Kabi USA, 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: | Fresenius Kabi USA, LLC |
NON-PROPRIETARY NAME: | THIAMINE HYDROCHLORIDE |
SUBSTANCE NAME: | THIAMINE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
DOSAGE FORM: | INJECTION, SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2000-09-01 |
END MARKETING DATE: | 0000-00-00 |
Thiamine HUMAN PRESCRIPTION DRUG Details:
Item Description | Thiamine from Fresenius Kabi USA, LLC |
LABELER NAME: | Fresenius Kabi USA, LLC |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 100(mg/mL) |
START MARKETING DATE: | 2000-09-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 63323-013_80e05c97-19b6-4cd5-81bf-6af1978bcf22 |
PRODUCT NDC: | 63323-013 |
APPLICATION NUMBER: | ANDA080556 |
Other THIAMINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: