Letomint (H&C 21 America Inc)
Welcome to the PulseAid listing for the Letomint drug offered from H&C 21 America Inc. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: | H&C 21 America Inc |
NON-PROPRIETARY NAME: | clove |
SUBSTANCE NAME: | CLOVE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2011-06-18 |
END MARKETING DATE: | 0000-00-00 |
Letomint HUMAN OTC DRUG Details:
Item Description | Letomint from H&C 21 America Inc |
LABELER NAME: | H&C 21 America Inc |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 18(mg/1) |
START MARKETING DATE: | 2011-06-18 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 76255-2001_dd69ed67-5608-4dbd-9543-48734bef70f7 |
PRODUCT NDC: | 76255-2001 |
APPLICATION NUMBER: | |
Other CLOVE Pharmaceutical Manufacturers / Labelers: