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FERROUS SULFATE
FERROUS SULFATE - 50436-5890-1 - (IRON SUPPLEMENT)
Drug Information of FERROUS SULFATE
| Product NDC: | 50436-5890 |
| Proprietary Name: | FERROUS SULFATE |
| Non Proprietary Name: | IRON SUPPLEMENT |
| Active Ingredient(s): | 325 mg/1 & nbsp; IRON SUPPLEMENT |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FERROUS SULFATE
| Product NDC: | 50436-5890 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20010219 |
Package Information of FERROUS SULFATE
| Package NDC: | 50436-5890-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (50436-5890-1) |
NDC Information of FERROUS SULFATE
| NDC Code | 50436-5890-1 |
| Proprietary Name | FERROUS SULFATE |
| Package Description | 30 TABLET in 1 BOTTLE (50436-5890-1) |
| Product NDC | 50436-5890 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IRON SUPPLEMENT |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010219 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Unit Dose Services |
| Substance Name | FERROUS SULFATE |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
