Dyural LM Kit (Asclemed USA, Inc.)
Welcome to the PulseAid listing for the Dyural LM 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: | Methylprednisolone Acetate, Lidocaine Hydrochloride, Bupivacaine Hydrochloride, Povidine Iodine, Isopropyl Alcohol |
SUBSTANCE NAME: | |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE; TOPICAL |
DOSAGE FORM: | KIT |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2014-08-21 |
END MARKETING DATE: | 0000-00-00 |
Dyural LM Kit HUMAN PRESCRIPTION DRUG Details:
Item Description | Dyural LM Kit from Asclemed USA, Inc. |
LABELER NAME: | Asclemed USA, Inc. |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | () |
START MARKETING DATE: | 2014-08-21 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 76420-795_7bbb8be2-d517-44e1-9af9-9ff539c1a61e |
PRODUCT NDC: | 76420-795 |
APPLICATION NUMBER: |