Product NDC: | 64376-809 |
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) |
Product NDC: | 64376-809 |
Labeler Name: | Boca Pharmacal, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100914 |
Package NDC: | 64376-809-10 |
Package Description: | 1000 TABLET in 1 BOTTLE (64376-809-10) |
NDC Code | 64376-809-10 |
Proprietary Name | Ferrous Sulfate |
Package Description | 1000 TABLET in 1 BOTTLE (64376-809-10) |
Product NDC | 64376-809 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ferrous Sulfate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100914 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Boca Pharmacal, Inc. |
Substance Name | FERROUS SULFATE |
Strength Number | 325 |
Strength Unit | mg/1 |
Pharmaceutical Classes |