Aspirin Tablet, Delayed Release
FDA Label NDC 50090-6929

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Aspirin (NDC 50090-6929). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, do not use, ask a doctor before use if, ask a doctor or pharmacist before use if you are, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

How Supplied

Product: 50090-6929

NDC: 50090-6929-0 120 TABLET, DELAYED RELEASE in a BOTTLE, PLASTIC / 1 in a CARTON

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