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Integra F
Integra F - 52747-711-60 - (Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid)
Drug Information of Integra F
| Product NDC: | 52747-711 |
| Proprietary Name: | Integra F |
| Non Proprietary Name: | Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Active Ingredient(s): | 40; 135.9; 191.2; 1; 3 mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp; Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Integra F
| Product NDC: | 52747-711 |
| Labeler Name: | US Pharmaceutical Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090427 |
Package Information of Integra F
| Package NDC: | 52747-711-60 |
| Package Description: | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-60) |
NDC Information of Integra F
| NDC Code | 52747-711-60 |
| Proprietary Name | Integra F |
| Package Description | 90 CAPSULE in 1 BOTTLE, PLASTIC (52747-711-60) |
| Product NDC | 52747-711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ferrous Fumarate and Polysacchride Iron Complex and Folic Acid |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090427 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | US Pharmaceutical Corporation |
| Substance Name | ASCORBIC ACID; FERROUS ASPARTO GLYCINATE; FERROUS FUMARATE; FOLIC ACID; NIACIN |
| Strength Number | 40; 135.9; 191.2; 1; 3 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient] |
