NDC Package 30698-335-01 Demerol

Meperidine Hydrochloride Tablet 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:
30698-335-01
Package Description:
100 TABLET in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Demerol
Non-Proprietary Name:
Meperidine Hydrochloride
Substance Name:
Meperidine Hydrochloride
Usage Information:
Meperidine is used to help relieve moderate to severe pain. It may also be used before and during surgery or other procedures. Meperidine belongs to a class of drugs known as opioid analgesics and is similar to morphine. It works in the brain to change how your body feels and responds to pain. Meperidine should not be used to treat long-term or ongoing pain. It should only be used to treat sudden episodes of moderate to severe pain. See also Precautions section.
11-Digit NDC Billing Format:
30698033501
NDC to RxNorm Crosswalk:
  • RxCUI: 861455 - meperidine HCl 100 MG Oral Tablet
  • RxCUI: 861455 - meperidine hydrochloride 100 MG Oral Tablet
  • RxCUI: 861455 - pethidine hydrochloride 100 MG Oral Tablet
  • RxCUI: 861467 - meperidine HCl 50 MG Oral Tablet
  • RxCUI: 861467 - meperidine hydrochloride 50 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Validus Pharmaceuticals Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA005010
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-10-1942
    Listing Expiration Date:
    12-31-2025
    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 30698-335-01?

    The NDC Packaged Code 30698-335-01 is assigned to a package of 100 tablet in 1 bottle, plastic of Demerol, a human prescription drug labeled by Validus Pharmaceuticals Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 30698-335 included in the NDC Directory?

    Yes, Demerol with product code 30698-335 is active and included in the NDC Directory. The product was first marketed by Validus Pharmaceuticals Llc on November 10, 1942 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 30698-335-01?

    The 11-digit format is 30698033501. 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
    5-3-230698-335-015-4-230698-0335-01