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  5. NDC Package Code: 71309-003-25 Adult Low Dose

NDC Package 71309-003-25 Adult Low Dose

Aspirin 81 Mg Tablet, Delayed Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
71309-003-25
Package Description:
25 POUCH in 1 BOX / 2 TABLET, DELAYED RELEASE in 1 POUCH
Product Code:
71309-003
Proprietary Name:
Adult Low Dose
Non-Proprietary Name:
Aspirin 81 Mg
Substance Name:
Aspirin
Usage Information:
Aspirin is used to reduce fever and relieve mild to moderate pain from conditions such as muscle aches, toothaches, common cold, and headaches. It may also be used to reduce pain and swelling in conditions such as arthritis. Aspirin is known as a salicylate and a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking a certain natural substance in your body to reduce pain and swelling. Consult your doctor before treating a child younger than 12 years. Your doctor may direct you to take a low dose of aspirin to prevent blood clots. This effect reduces the risk of stroke and heart attack. If you have recently had surgery on clogged arteries (such as bypass surgery, carotid endarterectomy, coronary stent), your doctor may direct you to use aspirin in low doses as a "blood thinner" to prevent blood clots.
11-Digit NDC Billing Format:
71309000325
NDC to RxNorm Crosswalk:
  • RxCUI: 308416 - aspirin 81 MG Delayed Release Oral Tablet
  • RxCUI: 308416 - ASA 81 MG Delayed Release Oral Tablet
  • RxCUI: 308416 - aspirin 81 MG Enteric Coated Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Safrel Pharmaceuticals, Llc.
    Dosage Form:
    Tablet, Delayed Release - A solid dosage form which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ASPIRIN 81 mg/1
    • Pharmacologic Class(es):
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Decreased Platelet Aggregation - [PE] (Physiologic Effect)
  • Decreased Prostaglandin Production - [PE] (Physiologic Effect)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
  • Platelet Aggregation Inhibitor - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    part343
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    02-09-2016
    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
    71309-003-022 POUCH in 1 POUCH / 2 TABLET, DELAYED RELEASE in 1 POUCH
    71309-003-05500 BOTTLE in 1 BOTTLE / 1000 BOTTLE in 1 BOTTLE (71309-003-01) / 365 BOTTLE in 1 BOTTLE (71309-003-65) / 30 CARTON in 1 BOTTLE (71309-003-30) / 1 TABLET, DELAYED RELEASE in 1 CARTON
    71309-003-101000 TABLET, DELAYED RELEASE in 1 BOTTLE
    71309-003-5050 POUCH in 1 BOX / 2 TABLET, DELAYED RELEASE in 1 POUCH
    71309-003-601 BOTTLE in 1 CARTON / 60 TABLET, DELAYED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71309-003-25?

    The NDC Packaged Code 71309-003-25 is assigned to a package of 25 pouch in 1 box / 2 tablet, delayed release in 1 pouch of Adult Low Dose, a human over the counter drug labeled by Safrel Pharmaceuticals, Llc.. The product's dosage form is tablet, delayed release and is administered via oral form.

    Is NDC 71309-003 included in the NDC Directory?

    Yes, Adult Low Dose with product code 71309-003 is active and included in the NDC Directory. The product was first marketed by Safrel Pharmaceuticals, Llc. on February 09, 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 71309-003-25?

    The 11-digit format is 71309000325. 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
    5-3-271309-003-255-4-271309-0003-25