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Ferrous Sulfate - 64376-809-10 - (Ferrous Sulfate)

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Drug Information of Ferrous Sulfate

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)

Labeler Information of Ferrous Sulfate

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 Information of Ferrous Sulfate

Package NDC: 64376-809-10
Package Description: 1000 TABLET in 1 BOTTLE (64376-809-10)

NDC Information of Ferrous Sulfate

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

Complete Information of Ferrous Sulfate


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