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Ferrous Sulfate
Ferrous Sulfate - 54738-963-13 - (Ferrous Sulfate)
Drug Information of Ferrous Sulfate
| Product NDC: | 54738-963 |
| Proprietary Name: | Ferrous Sulfate |
| Non Proprietary Name: | Ferrous Sulfate |
| Active Ingredient(s): | 325 mg/1 & nbsp; Ferrous Sulfate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ferrous Sulfate
| Product NDC: | 54738-963 |
| Labeler Name: | Richmond Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081105 |
Package Information of Ferrous Sulfate
| Package NDC: | 54738-963-13 |
| Package Description: | 100 TABLET in 1 BOTTLE (54738-963-13) |
NDC Information of Ferrous Sulfate
| NDC Code | 54738-963-13 |
| Proprietary Name | Ferrous Sulfate |
| Package Description | 100 TABLET in 1 BOTTLE (54738-963-13) |
| Product NDC | 54738-963 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ferrous Sulfate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081105 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Richmond Pharmaceuticals Inc. |
| Substance Name | FERROUS SULFATE |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
