NDC Package 71335-0062-2 Ergocalciferol

Capsule, Liquid Filled Oral - View Billable Units, 11-Digit Format, RxNorm

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:
71335-0062-2
Package Description:
30 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
Proprietary Name:
Ergocalciferol
Non-Proprietary Name:
Ergocalciferol
Substance Name:
Ergocalciferol
Usage Information:
Vitamin D (ergocalciferol-D2, cholecalciferol-D3, alfacalcidol) is a fat-soluble vitamin that helps your body absorb calcium and phosphorus. Having the right amount of vitamin D, calcium, and phosphorus is important for building and keeping strong bones. Vitamin D is used to treat and prevent bone disorders (such as rickets, osteomalacia). Vitamin D is made by the body when skin is exposed to sunlight. Sunscreen, protective clothing, limited exposure to sunlight, dark skin, and age may prevent getting enough vitamin D from the sun. Vitamin D with calcium is used to treat or prevent bone loss (osteoporosis). Vitamin D is also used with other medications to treat low levels of calcium or phosphate caused by certain disorders (such as hypoparathyroidism, pseudohypoparathyroidism, familial hypophosphatemia). It may be used in kidney disease to keep calcium levels normal and allow normal bone growth. Vitamin D drops (or other supplements) are given to breast-fed infants because breast milk usually has low levels of vitamin D.
11-Digit NDC Billing Format:
71335006202
NDC to RxNorm Crosswalk:
  • RxCUI: 1367410 - ergocalciferol 1.25 MG (50,000 UNT) Oral Capsule
  • RxCUI: 1367410 - ergocalciferol 1.25 MG Oral Capsule
  • RxCUI: 1367410 - vitamin D 1.25 MG Oral Capsule
  • RxCUI: 1367410 - vitamin D2 1250 MCG Oral Capsule
  • RxCUI: 1367410 - vitamin D2 50,000 UNT Oral Capsule
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bryant Ranch Prepack
    Dosage Form:
    Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA080704
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-15-2016
    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
    71335-0062-045 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-112 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-3100 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-44 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-520 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-68 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-715 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-8120 CAPSULE, LIQUID FILLED in 1 BOTTLE
    71335-0062-960 CAPSULE, LIQUID FILLED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71335-0062-2?

    The NDC Packaged Code 71335-0062-2 is assigned to a package of 30 capsule, liquid filled in 1 bottle of Ergocalciferol, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is capsule, liquid filled and is administered via oral form.

    Is NDC 71335-0062 included in the NDC Directory?

    Yes, Ergocalciferol with product code 71335-0062 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on June 15, 2016 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 71335-0062-2?

    The 11-digit format is 71335006202. 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 5-4-1 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
    5-4-171335-0062-25-4-271335-0062-02