Marbeta L Kit (Asclemed USA, Inc.)
Welcome to the PulseAid listing for the Marbeta L Kit drug offered from Asclemed USA, 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: | Asclemed USA, Inc. |
NON-PROPRIETARY NAME: | Betamethasone Sodium Phosphate, Betamethasone Acetate, Lidocaine Hydrochloride, Bupivacaine Hydrochloride, Povidine Iodine, Isopropyl Alcohol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; TOPICAL |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2010-04-28 |
END MARKETING DATE: | 0000-00-00 |
Marbeta L Kit HUMAN PRESCRIPTION DRUG Details:
Item Description | Marbeta L Kit from Asclemed USA, Inc. |
LABELER NAME: | Asclemed USA, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2010-04-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 76420-782_0fd0bf76-5ab1-4c64-b13c-3a53d28c5462 |
PRODUCT NDC: | 76420-782 |
APPLICATION NUMBER: |