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Choice OB DHA - 42192-353-60 - (.beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent)

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Drug Information of Choice OB DHA

Product NDC: 42192-353
Proprietary Name: Choice OB DHA
Non Proprietary Name: .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent
Active Ingredient(s):    & nbsp;   .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Choice OB DHA

Product NDC: 42192-353
Labeler Name: Acella Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20130517

Package Information of Choice OB DHA

Package NDC: 42192-353-60
Package Description: 30 BLISTER PACK in 1 CARTON (42192-353-60) > 1 KIT in 1 BLISTER PACK

NDC Information of Choice OB DHA

NDC Code 42192-353-60
Proprietary Name Choice OB DHA
Package Description 30 BLISTER PACK in 1 CARTON (42192-353-60) > 1 KIT in 1 BLISTER PACK
Product NDC 42192-353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name .beta.-carotene, cholecalciferol, ascorbic acid, .alpha.-tocopherol acetate, dl-, folic acid, thiamine mononitrate, riboflavin, pyridoxine hydrochloride, cyanocobalamin, niacinamide, calcium carbonate, ferrous fumarate, magnesium oxide, zinc oxide, cupric oxide and doconexent
Dosage Form Name KIT
Route Name
Start Marketing Date 20130517
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella Pharmaceuticals, LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Choice OB DHA


General Information