HEMATOGEN - 63044-631-19 - (HEMATOGEN)

Alphabetical Index


Drug Information of HEMATOGEN

Product NDC: 63044-631
Proprietary Name: HEMATOGEN
Non Proprietary Name: HEMATOGEN
Active Ingredient(s): 250; 10; 200    mg/1; ug/1; mg/1 & nbsp;   HEMATOGEN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of HEMATOGEN

Product NDC: 63044-631
Labeler Name: Nnodum Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070510

Package Information of HEMATOGEN

Package NDC: 63044-631-19
Package Description: 10 BLISTER PACK in 1 BOX (63044-631-19) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of HEMATOGEN

NDC Code 63044-631-19
Proprietary Name HEMATOGEN
Package Description 10 BLISTER PACK in 1 BOX (63044-631-19) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 63044-631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HEMATOGEN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070510
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Nnodum Pharmaceuticals
Substance Name ASCORBIC ACID; CYANOCOBALAMIN; FERROUS FUMARATE
Strength Number 250; 10; 200
Strength Unit mg/1; ug/1; mg/1
Pharmaceutical Classes Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of HEMATOGEN


General Information