NDC 33261-152 Adult Low Dose Aspirin

NDC Product Code 33261-152

NDC CODE: 33261-152

Proprietary Name: Adult Low Dose Aspirin What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Product Characteristics

Color(s):
YELLOW (C48330 - YELLOW COLOR)
Shape: ROUND (C48348)
Size(s):
8 MM
Imprint(s):
PH023
Score: 1

NDC Code Structure

NDC 33261-152-00

Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

NDC 33261-152-09

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (33261-152-30)

NDC 33261-152-60

Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

NDC 33261-152-90

Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

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

NDC Product Information

Adult Low Dose Aspirin with NDC 33261-152 is a product labeled by Aidarex Pharmaceuticals Llc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 308416.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • HYPROMELLOSES (UNII: 3NXW29V3WO)
  • METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • STARCH, CORN (UNII: O8232NY3SJ)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • TALC (UNII: 7SEV7J4R1U)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Aidarex Pharmaceuticals Llc
Labeler Code: 33261
Start Marketing Date: 01-12-2007 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Information for Patients

Aspirin

Aspirin is pronounced as (as' pir in)

Why is aspirin medication prescribed?
Prescription aspirin is used to relieve the symptoms of rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), osteoarthritis (arthritis caused ...
[Read More]

* Please review the disclaimer below.

Adult Low Dose Aspirin Product Label Images

Adult Low Dose Aspirin Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient (In Each Tablet):

Aspirin 81mg (NSAID)**nonsteroidal anti-inflammatory drug

Purpose

Pain reliever

Do Not Use If

You have ever had an allergic reaction to aspirin or any other pain reliever/fever reducer

Ask A Doctor Before Use If

  • The stomach bleeding warning applies to youyou have a history of stomach problems such as heartburnyou have high blood pressure, heart disease, liver cirrhosis or kidney diseaseyou have asthmayou are taking a diuretic

Ask A Doctor Or Pharmacist Before Use If You Are Taking A Prescription Drug For:

  • Goutdiabetesarthritis

Stop Use And Ask A Doctor If:

  • You experience any of the following signs of stomach bleeding: feel faint, vomit blood, have bloody or black stools, have stomach pain that does not get betterallergic reaction occurspain gets worse or lasts more than 10 daysredness or swelling is present any new symptoms occurringing in the ears or loss of hearing occursThese could be signs of a serious condition.

If Pregnant Or Breast-Feeding,

Ask a health professional before use. It is especially important not to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

Keep Out Of Reach Of Children.

In case of accidental overdose, get medical help or contact a Poison Control Center right away.

Directions:

  • Drink a full glass of water with each doseadults and children 12 years and over: take 4 to 8 tablets every 4 hours while symptoms persist. Do not to exceed 48 tablets in 24 hors or as directed by a physicianchildren under 12 years: consult a physician

Other Information

  • Tamper Evident: Do not use if safety seal under cap is broken or missingstore at room temperature (15°-30°C)avoid excess heat and moisture

Questions?

Adverse drug event call: (866) 562-2756

* Please review the disclaimer below.