| PRODUCT NDC | 61919-042 | The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| PROPRIETARY NAME | DULOXETINE HYDROCHLORIDE | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
| START MARKETING DATE | 8/16/2019 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| LABELER NAME | Direct_Rx | Name of Company corresponding to the labeler code segment of the Product NDC. |
| PRODUCT NDC | 61919-042 | The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| PROPRIETARY NAME | DULOXETINE HYDROCHLORIDE | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
| START MARKETING DATE | 1/1/2014 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
| LABELER NAME | DIRECT RX | Name of Company corresponding to the labeler code segment of the Product NDC. |