Drugplain

Quality Choice Extra Strength Effervescent Antacid and Pain Relief 1000 mg/1

Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate · TABLET, EFFERVESCENT · Chain Drug Marketing Association

No Recall History
Plain English

Quality Choice Extra Strength Effervescent Antacid and Pain Relief is a tablet, effervescent containing aspirin, anhydrous citric acid, sodium bicarbonate at 1000 mg/1, taken oral. Manufactured by Chain Drug Marketing Association.

Key Facts

Brand Name
Quality Choice Extra Strength Effervescent Antacid and Pain Relief
Generic Name
Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate
NDC Code (Product)
63868-569
Manufacturer
Chain Drug Marketing Association
Strength
1000 mg/1
Dosage Form
TABLET, EFFERVESCENT
Route
ORAL
Marketing Status
Application #
M013
Drug Class
Calculi Dissolution Agent [EPC]; Anti-coagulant [EPC]
Marketing Start
11/04/2020

Recall History

No Recall History

Frequently Asked Questions

What is Quality Choice Extra Strength Effervescent Antacid and Pain Relief used for?

Quality Choice Extra Strength Effervescent Antacid and Pain Relief contains Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate. It is a tablet, effervescent taken oral. Consult your doctor for specific uses.

Is Quality Choice Extra Strength Effervescent Antacid and Pain Relief a controlled substance?

Quality Choice Extra Strength Effervescent Antacid and Pain Relief is not classified as a controlled substance by the DEA.

What is the generic name for Quality Choice Extra Strength Effervescent Antacid and Pain Relief?

The generic name for Quality Choice Extra Strength Effervescent Antacid and Pain Relief is Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate. There are 1 other brand versions of Aspirin, Anhydrous Citric Acid, Sodium Bicarbonate.

What is the NDC code for Quality Choice Extra Strength Effervescent Antacid and Pain Relief 1000 mg/1?

The NDC (National Drug Code) for Quality Choice Extra Strength Effervescent Antacid and Pain Relief 1000 mg/1 is 63868-569, listed by Chain Drug Marketing Association.

Product NDC

63868-569

Package NDC

63868-569-24

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)