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  5. NDC Package Code: 52747-620-10 Concept Ob

NDC Package 52747-620-10 Concept Ob

Vitamin Mineral Supplement Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
52747-620-10
Package Description:
10 BLISTER PACK in 1 BOX / 4 CAPSULE in 1 BLISTER PACK (52747-620-04)
Product Code:
52747-620
Proprietary Name:
Concept Ob
Non-Proprietary Name:
Vitamin Mineral Supplement
Substance Name:
Ascorbic Acid; Biotin; Calcium Pantothenate; Cupric Sulfate; Cyanocobalamin; Ferrous Fumarate; Folic Acid; Iron; Magnesium Sulfate, Unspecified Form; Manganese Sulfate; Niacin; Pyridoxine Hydrochloride; Riboflavin; Thiamine Mononitrate; Zinc Sulfate, Unspecified Form
Usage Information:
This medication is a multivitamin and iron product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins and iron are important building blocks of the body and help keep you in good health.
11-Digit NDC Billing Format:
52747062010
NDC to RxNorm Crosswalk:
  • RxCUI: 1314666 - ascorbic acid 210 MG / biotin 0.3 MG / calcium pantothenate 7 MG / copper sulfate 0.8 MG / ferrous fumarate 130 MG / folic acid 1 MG / magnesium sulfate 6.9 MG / manganese sulfate 1.3 MG / niacin 20 MG / polysaccharide iron complex 92.4 MG / pyridoxine hydrochloride 25 MG / riboflavin 5 MG / thiamine mononitrate 5 MG / vitamin B12 0.01 MG / zinc sulfate 18.2 MG Oral Capsule
  • RxCUI: 1314666 - vitamin C 210 MG / biotin 0.3 MG / calcium pantothenate 7 MG / copper sulfate 0.8 MG / ferrous fumarate 130 MG / folate 1 MG / magnesium sulfate 6.9 MG / manganese sulfate 1.3 MG / nicotinic acid 20 MG / polysaccharide iron complex 92.4 MG / vitamin B6 hydrochloride 25 MG / riboflavin 5 MG / vitamin B1 mononitrate 5 MG / vitamin B12 0.01 MG / ZnSO4 18.2 MG Oral Capsule
  • RxCUI: 1314666 - vitamin C 210 MG / biotin 0.3 MG / calcium pantothenate 7 MG / copper sulfate 0.8 MG / ferrous fumarate 130 MG / folate 1 MG / magnesium sulfate 6.9 MG / manganese sulfate 1.3 MG / nicotinic acid 20 MG / polysaccharide iron complex 92.4 MG / vitamin B6 hydrochloride 25 MG / riboflavin 5 MG / vit-B1 mononitrate 5 MG / vitamin B12 0.01 MG / ZnSO4 18.2 MG Oral Capsule
  • RxCUI: 1314666 - vitamin C 210 MG / biotin 0.3 MG / calcium pantothenate 7 MG / copper sulfate 0.8 MG / ferrous fumarate 130 MG / folate 1 MG / magnesium sulfate 6.9 MG / manganese sulfate 1.3 MG / nicotinic acid 20 MG / polysaccharide iron complex 92.4 MG / vit-B6 hydrochloride 25 MG / riboflavin 5 MG / vitamin B1 mononitrate 5 MG / vitamin B12 0.01 MG / ZnSO4 18.2 MG Oral Capsule
  • RxCUI: 1314666 - vitamin C 210 MG / biotin 0.3 MG / calcium pantothenate 7 MG / copper sulfate 0.8 MG / ferrous fumarate 130 MG / folate 1 MG / magnesium sulfate 6.9 MG / manganese sulfate 1.3 MG / nicotinic acid 20 MG / polysaccharide iron complex 92.4 MG / vit-B6 hydrochloride 25 MG / riboflavin 5 MG / vit-B1 mononitrate 5 MG / vitamin B12 0.01 MG / ZnSO4 18.2 MG Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    U.s. Pharmaceutical Corporation
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ASCORBIC ACID 210 mg/1
  • BIOTIN 300 ug/1
  • CALCIUM PANTOTHENATE 7 mg/1
  • CUPRIC SULFATE 800 ug/1
  • CYANOCOBALAMIN 10 ug/1
  • FERROUS FUMARATE 42.5 mg/1
  • FOLIC ACID 1 mg/1
  • IRON 42.5 mg/1
  • MAGNESIUM SULFATE, UNSPECIFIED FORM 6.9 mg/1
  • MANGANESE SULFATE 1.3 mg/1
  • NIACIN 20 mg/1
  • PYRIDOXINE HYDROCHLORIDE 25 mg/1
  • RIBOFLAVIN 5 mg/1
  • THIAMINE MONONITRATE 5 mg/1
  • ZINC SULFATE, UNSPECIFIED FORM 18.2 mg/1
    • Pharmacologic Class(es):
  • Analogs/Derivatives - [Chemical/Ingredient]
  • Ascorbic Acid - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Magnetic Resonance Contrast Activity - [MoA] (Mechanism of Action)
  • Nicotinic Acid - [EPC] (Established Pharmacologic Class)
  • Nicotinic Acids - [CS]
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Paramagnetic Contrast Agent - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin B 12 - [CS]
  • Vitamin B 6 - [Chemical/Ingredient]
  • Vitamin B12 - [EPC] (Established Pharmacologic Class)
  • Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-01-2009
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    52747-620-3030 CAPSULE in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52747-620-10?

    The NDC Packaged Code 52747-620-10 is assigned to a package of 10 blister pack in 1 box / 4 capsule in 1 blister pack (52747-620-04) of Concept Ob, a human prescription drug labeled by U.s. Pharmaceutical Corporation. The product's dosage form is capsule and is administered via oral form.

    Is NDC 52747-620 included in the NDC Directory?

    Yes, Concept Ob with product code 52747-620 is active and included in the NDC Directory. The product was first marketed by U.s. Pharmaceutical Corporation on January 01, 2009 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52747-620-10?

    The 11-digit format is 52747062010. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-252747-620-105-4-252747-0620-10