Ferrous Sulfate (Sun Pharmaceutical Industries, Inc.)
Welcome to the PulseAid listing for the Ferrous Sulfate drug offered from Sun Pharmaceutical Industries, 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: | Sun Pharmaceutical Industries, Inc. |
| NON-PROPRIETARY NAME: | Ferrous Sulfate |
| SUBSTANCE NAME: | FERROUS SULFATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2014-07-01 |
| END MARKETING DATE: | 0000-00-00 |
Ferrous Sulfate HUMAN OTC DRUG Details:
| Item Description | Ferrous Sulfate from Sun Pharmaceutical Industries, Inc. |
| LABELER NAME: | Sun Pharmaceutical Industries, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 325(mg/1) |
| START MARKETING DATE: | 2014-07-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 57664-070_bca6e06f-e9ea-4957-af87-453044fbf10b |
| PRODUCT NDC: | 57664-070 |
| APPLICATION NUMBER: | |
Other FERROUS SULFATE Pharmaceutical Manufacturers / Labelers:
