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FERROUS SULFATE - 68210-1520-3 - (FERROUS SULFATE, DRIED)

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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

Complete Information of FERROUS SULFATE


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