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  5. NDC Package Code: 72275-741-77 Clindavix

NDC Package 72275-741-77 Clindavix

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
72275-741-77
Package Description:
1 KIT in 1 CARTON * 60 mL in 1 BOTTLE, WITH APPLICATOR * 114 g in 1 TUBE
Product Code:
72275-741
Proprietary Name:
Clindavix
Usage Information:
Clindamycin Phosphate Topical Solution USP, 1% is indicated in the treatment of acne vulgaris. In view of the potential for diarrhea, bloody diarrhea and pseudomembranous colitis, the physician should consider whether other agents are more appropriate (see CONTRAINDICATIONS, WARNINGS and ADVERSE REACTIONS).
11-Digit NDC Billing Format:
72275074177
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1591982 - dimethicone 1.8 % / zinc oxide 2 % Topical Ointment
  • RxCUI: 1591982 - dimethicone 0.018 MG/MG / zinc oxide 0.02 MG/MG Topical Ointment
  • RxCUI: 1591982 - dimethicone 0.018 MG/MG / ZNO 0.02 MG/MG Topical Ointment
  • RxCUI: 2530889 - Dynashield (dimethicone 1.8 % / zinc oxide 2 % ) Topical Ointment
  • RxCUI: 2530889 - dimethicone 0.018 MG/MG / zinc oxide 0.02 MG/MG Topical Ointment [Dynashield]
    • Labeler Name:
    Primary Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    09-17-2013
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 72275-741-77?

    The NDC Packaged Code 72275-741-77 is assigned to a package of 1 kit in 1 carton * 60 ml in 1 bottle, with applicator * 114 g in 1 tube of Clindavix, labeled by Primary Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 72275-741 included in the NDC Directory?

    No, Clindavix with product code 72275-741 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Primary Pharmaceuticals, Inc. on September 17, 2013 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 72275-741-77?

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

    What is the 11-digit format for NDC 72275-741-77?

    The 11-digit format is 72275074177. 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
    5-3-272275-741-775-4-272275-0741-77