NDC Package 16714-121-01 Pilocarpine Hydrochloride

Tablet, Film Coated 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:
16714-121-01
Package Description:
100 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Pilocarpine Hydrochloride
Non-Proprietary Name:
Pilocarpine Hydrochloride
Substance Name:
Pilocarpine Hydrochloride
Usage Information:
INDICATIONS AND USAGEPilocarpine hydrochloride tablets are indicated for 1) the treatment of symptoms of dry mouth from salivary gland hypofunction caused by radiotherapy for cancer of the head and neck; and 2) the treatment of symptoms of dry mouth in patients with Sjogren's Syndrome.
11-Digit NDC Billing Format:
16714012101
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
100 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1000913 - pilocarpine HCl 5 MG Oral Tablet
  • RxCUI: 1000913 - pilocarpine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1001004 - pilocarpine HCl 7.5 MG Oral Tablet
  • RxCUI: 1001004 - pilocarpine hydrochloride 7.5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Northstar Rx Llc
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA212377
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-13-2019
    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.

    Frequently Asked Questions

    What is NDC 16714-121-01?

    The NDC Packaged Code 16714-121-01 is assigned to a package of 100 tablet, film coated in 1 bottle of Pilocarpine Hydrochloride, a human prescription drug labeled by Northstar Rx Llc. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 16714-121 included in the NDC Directory?

    Yes, Pilocarpine Hydrochloride with product code 16714-121 is active and included in the NDC Directory. The product was first marketed by Northstar Rx Llc on August 13, 2019 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 NDC billing unit for package 16714-121-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 100.

    What is the 11-digit format for NDC 16714-121-01?

    The 11-digit format is 16714012101. 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
    5-3-216714-121-015-4-216714-0121-01