Felbamate Tablet
FDA Label NDC 70771-1077

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Felbamate (NDC 70771-1077). 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 70771-1077-1

Felbamate tablets USP, 400 mg

100 Tablets

Rx only

Labels (54e4d1c3 Cf8c 4fff 8280 8edcb484c76e 02)

Labels (54e4d1c3 Cf8c 4fff 8280 8edcb484c76e 02)

NDC 70771-1078-1

Felbamate tablets USP, 600 mg

100 Tablets

Rx only

Labels (54e4d1c3 Cf8c 4fff 8280 8edcb484c76e 03)

Labels (54e4d1c3 Cf8c 4fff 8280 8edcb484c76e 03)

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