EDP INDIGO (EDP Inc.)
Welcome to the PulseAid listing for the EDP INDIGO drug offered from EDP 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: | EDP Inc. |
| NON-PROPRIETARY NAME: | Indigofera Tinctoria Leaf |
| SUBSTANCE NAME: | INDIGOFERA TINCTORIA LEAF |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | POWDER |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2016-02-01 |
| END MARKETING DATE: | 0000-00-00 |
EDP INDIGO HUMAN OTC DRUG Details:
| Item Description | EDP INDIGO from EDP Inc. |
| LABELER NAME: | EDP Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.999(1/100g) |
| START MARKETING DATE: | 2016-02-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 70434-102_3a5e67b1-1cc0-46de-bc0b-58c8e7d0f3fd |
| PRODUCT NDC: | 70434-102 |
| APPLICATION NUMBER: | |
Other INDIGOFERA TINCTORIA LEAF Pharmaceutical Manufacturers / Labelers:
