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FERROUS SULFATE
FERROUS SULFATE - 68210-1520-3 - (FERROUS SULFATE, DRIED)
Drug Information of FERROUS SULFATE
| Product NDC: | 68210-1520 |
| Proprietary Name: | FERROUS SULFATE |
| Non Proprietary Name: | FERROUS SULFATE, DRIED |
| Active Ingredient(s): | 325 mg/1 & nbsp; FERROUS SULFATE, DRIED |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FERROUS SULFATE
| Product NDC: | 68210-1520 |
| Labeler Name: | SPIRIT PHARMACEUTICALS,LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101215 |
Package Information of FERROUS SULFATE
| Package NDC: | 68210-1520-3 |
| Package Description: | 1 BAG in 1 DRUM (68210-1520-3) > 1000 TABLET, FILM COATED in 1 BAG |
NDC Information of FERROUS SULFATE
| NDC Code | 68210-1520-3 |
| Proprietary Name | FERROUS SULFATE |
| Package Description | 1 BAG in 1 DRUM (68210-1520-3) > 1000 TABLET, FILM COATED in 1 BAG |
| Product NDC | 68210-1520 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | FERROUS SULFATE, DRIED |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101215 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | SPIRIT PHARMACEUTICALS,LLC |
| Substance Name | FERROUS SULFATE, DRIED |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
