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FERROUS SULFATE
FERROUS SULFATE - 53807-177-08 - (FERROUS SULFATE)
Drug Information of FERROUS SULFATE
| Product NDC: | 53807-177 |
| Proprietary Name: | FERROUS SULFATE |
| Non Proprietary Name: | FERROUS SULFATE |
| Active Ingredient(s): | 220 mg/5mL & nbsp; FERROUS SULFATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | ELIXIR |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FERROUS SULFATE
| Product NDC: | 53807-177 |
| Labeler Name: | Rij Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19990316 |
Package Information of FERROUS SULFATE
| Package NDC: | 53807-177-08 |
| Package Description: | 236 mL in 1 BOTTLE (53807-177-08) |
NDC Information of FERROUS SULFATE
| NDC Code | 53807-177-08 |
| Proprietary Name | FERROUS SULFATE |
| Package Description | 236 mL in 1 BOTTLE (53807-177-08) |
| Product NDC | 53807-177 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | FERROUS SULFATE |
| Dosage Form Name | ELIXIR |
| Route Name | ORAL |
| Start Marketing Date | 19990316 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rij Pharmaceutical Corporation |
| Substance Name | FERROUS SULFATE |
| Strength Number | 220 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
