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 DescriptionLetomint 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:

Manufacturer / LabelerProprietary Name
Antigen Laboratories, Inc.Clove
H&C 21 America IncLetomint
JMBio Co., Ltd.JAMU Sexty
Nelco Laboratories, Inc.Cloves
SOMA Biotechnology Co., LtdSOMA Circum
US EXCY-LINE INC.Nose