72835-660 NDC - MATERVIA (ASCORBIC ACID, CHOLECALCIFEROL, THIAMINE, PYRIDOXAL-5-PHOSPHATE, FOLIC ACID, METHYLCOBALAMIN, CALCIUM CITRATE, IRON, IODINE)

Drug Information

  • Product NDC: 72835-660
  • Proprietary Name: Matervia
  • Non Proprietary Name: ascorbic acid, cholecalciferol, thiamine, pyridoxal-5-phosphate, folic acid, methylcobalamin, calcium citrate, iron, iodine
  • Active Ingredient(s): 125 mg/1 ASCORBIC ACID; 200 mg/1 CALCIUM CITRATE; 20 ug/1 CHOLECALCIFEROL; 1000 ug/1 FOLIC ACID; 13 mg/1 IRON; 1000 ug/1 METHYLCOBALAMIN; 150 ug/1 POTASSIUM IODIDE; 2.5 mg/1 PYRIDOXAL 5-PHOSPHATE; 1.4 mg/1 THIAMINE MONONITRATE
  • Administration Route(s): ORAL
  • Dosage Form(s): CAPSULE
  • Pharmacy Class(es): Ascorbic Acid [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Increased Coagulation Factor Activity [PE]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name Field Value
Labeler Name: V2 Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:6/11/2025

Package Information

No. Package Code Package Description Billing Unit
172835-660-0160 CAPSULE in 1 BOTTLE (72835-660-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC72835-660The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEMaterviaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEascorbic acid, cholecalciferol, thiamine, pyridoxal-5-phosphate, folic acid, methylcobalamin, calcium citrate, iron, iodineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/11/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEV2 Pharma LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEASCORBIC ACID; CALCIUM CITRATE; CHOLECALCIFEROL; FOLIC ACID; IRON; METHYLCOBALAMIN; POTASSIUM IODIDE; PYRIDOXAL 5-PHOSPHATE; THIAMINE MONONITRATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH125; 200; 20; 1000; 13; 1000; 150; 2.5; 1.4 
ACTIVE INGRED UNITmg/1; mg/1; ug/1; ug/1; mg/1; ug/1; ug/1; mg/1; mg/1 
PHARM CLASSESAscorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC] 

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This page was last updated on: 12/6/2025

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