Prenate AM - 75854-307-30 - (.pyridoxine hydrochloride, cyanocobalamin, calcium carbonate and folic acid)

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Drug Information of Prenate AM

Product NDC: 75854-307
Proprietary Name: Prenate AM
Non Proprietary Name: .pyridoxine hydrochloride, cyanocobalamin, calcium carbonate and folic acid
Active Ingredient(s): 200; 12; 1; 75    mg/1; ug/1; mg/1; mg/1 & nbsp;   .pyridoxine hydrochloride, cyanocobalamin, calcium carbonate and folic acid
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Prenate AM

Product NDC: 75854-307
Labeler Name: Avion Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20130615

Package Information of Prenate AM

Package NDC: 75854-307-30
Package Description: 30 TABLET, COATED in 1 BOTTLE (75854-307-30)

NDC Information of Prenate AM

NDC Code 75854-307-30
Proprietary Name Prenate AM
Package Description 30 TABLET, COATED in 1 BOTTLE (75854-307-30)
Product NDC 75854-307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name .pyridoxine hydrochloride, cyanocobalamin, calcium carbonate and folic acid
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130615
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Avion Pharmaceuticals, LLC
Substance Name CALCIUM CARBONATE; CYANOCOBALAMIN; FOLIC ACID; PYRIDOXINE HYDROCHLORIDE
Strength Number 200; 12; 1; 75
Strength Unit mg/1; ug/1; mg/1; mg/1
Pharmaceutical Classes Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient]

Complete Information of Prenate AM


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