NDC Package 62207-773-58 Ranitidine

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:
62207-773-58
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Ranitidine
Non-Proprietary Name:
Ranitidine
Substance Name:
Ranitidine Hydrochloride
Usage Information:
◾ adults and children 12 years and over:    ◾ to relieve symptoms, swallow 1 tablet with a glass of water    ◾ to prevent symptoms, swallow 1 tablet with a glass of water ​30 to 60 minutes before​ eating food or drinking beverages that cause heartburn    ◾ can be used up to twice daily (do not take more than 2 tablets in 24 hours)    ◾ do not chew tablet (for cool mint tablets only) ◾ children under 12 years: ask a doctor
11-Digit NDC Billing Format:
62207077358
NDC to RxNorm Crosswalk:
  • RxCUI: 198191 - ranitidine 150 MG Oral Tablet
  • RxCUI: 198191 - ranitidine 150 MG (as ranitidine HCl 168 MG) Oral Tablet
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Granules India Ltd
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA210243
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-26-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    62207-773-365 BAG in 1 CARTON / 10000 TABLET in 1 BAG (62207-773-32)
    62207-773-411 BOTTLE in 1 CARTON / 24 TABLET in 1 BOTTLE
    62207-773-471 BOTTLE in 1 CARTON / 500 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 62207-773-58?

    The NDC Packaged Code 62207-773-58 is assigned to a package of 2 blister pack in 1 carton / 10 tablet in 1 blister pack of Ranitidine, a human over the counter drug labeled by Granules India Ltd. The product's dosage form is tablet and is administered via oral form.

    Is NDC 62207-773 included in the NDC Directory?

    Yes, Ranitidine with product code 62207-773 is active and included in the NDC Directory. The product was first marketed by Granules India Ltd on June 26, 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 11-digit format for NDC 62207-773-58?

    The 11-digit format is 62207077358. 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
    5-3-262207-773-585-4-262207-0773-58