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Hematogen FA - 63044-632-17 - (Hematogen FA)

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Drug Information of Hematogen FA

Product NDC: 63044-632
Proprietary Name: Hematogen FA
Non Proprietary Name: Hematogen FA
Active Ingredient(s): 250; 10; 200; 1    mg/1; ug/1; mg/1; mg/1 & nbsp;   Hematogen FA
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Hematogen FA

Product NDC: 63044-632
Labeler Name: Nnodum Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050101

Package Information of Hematogen FA

Package NDC: 63044-632-17
Package Description: 10 BLISTER PACK in 1 BOX (63044-632-17) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Hematogen FA

NDC Code 63044-632-17
Proprietary Name Hematogen FA
Package Description 10 BLISTER PACK in 1 BOX (63044-632-17) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 63044-632
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hematogen FA
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Nnodum Pharmaceuticals
Substance Name ASCORBIC ACID; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID
Strength Number 250; 10; 200; 1
Strength Unit mg/1; ug/1; mg/1; mg/1
Pharmaceutical Classes Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of Hematogen FA


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