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HemeNatal OB - 76331-901-90 - (CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL SUCCINATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, CALCIUM PANTOTHENATE, IRON SUCROSE, HEME IRON POLYPEPTIDE, POTASSIUM IODIDE, ZINC OXIDE, SODIUM SELENATE, CUPRIC SULFATE)

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Drug Information of HemeNatal OB

Product NDC: 76331-901
Proprietary Name: HemeNatal OB
Non Proprietary Name: CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL SUCCINATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, CALCIUM PANTOTHENATE, IRON SUCROSE, HEME IRON POLYPEPTIDE, POTASSIUM IODIDE, ZINC OXIDE, SODIUM SELENATE, CUPRIC SULFATE
Active Ingredient(s): 10; 30; 10; 400; .8; 12; 1; 6; 28; 17; 250; 50; 1.6; 65; 1.5; 4.5    [iU]/1; ug/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1 & nbsp;   CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL SUCCINATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, CALCIUM PANTOTHENATE, IRON SUCROSE, HEME IRON POLYPEPTIDE, POTASSIUM IODIDE, ZINC OXIDE, SODIUM SELENATE, CUPRIC SULFATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of HemeNatal OB

Product NDC: 76331-901
Labeler Name: WH Nutritionals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120308

Package Information of HemeNatal OB

Package NDC: 76331-901-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (76331-901-90)

NDC Information of HemeNatal OB

NDC Code 76331-901-90
Proprietary Name HemeNatal OB
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (76331-901-90)
Product NDC 76331-901
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL SUCCINATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, BIOTIN, CALCIUM PANTOTHENATE, IRON SUCROSE, HEME IRON POLYPEPTIDE, POTASSIUM IODIDE, ZINC OXIDE, SODIUM SELENATE, CUPRIC SULFATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120308
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name WH Nutritionals, LLC
Substance Name .ALPHA.-TOCOPHEROL SUCCINATE, D-; BIOTIN; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; CUPRIC SULFATE; CYANOCOBALAMIN; FOLIC ACID; HEME IRON POLYPEPTIDE; IRON SUCROSE; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM SELENATE; THIAMINE MONONITRATE; ZINC OXIDE
Strength Number 10; 30; 10; 400; .8; 12; 1; 6; 28; 17; 250; 50; 1.6; 65; 1.5; 4.5
Strength Unit [iU]/1; ug/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

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