Prucalopride Tablet, Film Coated
FDA Label NDC 70771-1900

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Prucalopride (NDC 70771-1900). 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 package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

NDC 70771-1899-3

Prucalopride Tablets

1 mg tablet

30 Tablets

Rx only

1 mg Label (051f4f7e 88e8 4706 8183 Dbd3f9d42d72 01)

NDC 70771-1900-3

Prucalopride Tablets

2 mg tablet

30 Tablets

Rx only

2 mg Label (051f4f7e 88e8 4706 8183 Dbd3f9d42d72 02)

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