42192-320 NDC - PNV-SELECT ()

Drug Information

  • Product NDC: 42192-320
  • Proprietary Name: PNV-Select
  • Non Proprietary Name:
  • Active Ingredient(s): 10 [iU]/1 .ALPHA.-TOCOPHEROL ACETATE, DL-; 80 mg/1 ASCORBIC ACID; 300 ug/1 BIOTIN; 120 mg/1 CALCIUM CARBONATE; 6 mg/1 CALCIUM PANTOTHENATE; 400 [iU]/1 CHOLECALCIFEROL; 2 mg/1 CUPRIC OXIDE; 12 ug/1 CYANOCOBALAMIN; 27 mg/1 FERROUS FUMARATE; 1 mg/1 FOLIC ACID; 30 ug/1 MAGNESIUM OXIDE; 20 mg/1 NIACINAMIDE; 150 ug/1 POTASSIUM IODIDE; 20 mg/1 PYRIDOXINE HYDROCHLORIDE; 3.4 mg/1 RIBOFLAVIN; 3 mg/1 THIAMINE MONONITRATE; 2500 [iU]/1 VITAMIN A ACETATE; 15 ug/1 ZINC OXIDE
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Increased Coagulation Factor Activity [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]; Vitamin A [CS]; Vitamin A [EPC]; Vitamin B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Acella Pharmaceuticals, LLC
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:10/15/2015
End Marketing Date:6/30/2017

Package Information

No. Package Code Package Description Billing Unit
142192-320-3030 TABLET, FILM COATED in 1 BOTTLE (42192-320-30)EA
242192-320-9090 TABLET, FILM COATED in 1 BOTTLE (42192-320-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC42192-320The 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.
PROPRIETARY NAMEPNV-SelectThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/15/2015This 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 NAMEAcella Pharmaceuticals, LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC42192-320The 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.
PROPRIETARY NAMEPNV-SelectThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/1/1990This 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 NAMEAcella Pharmaceuticals, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 3/6/2026

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