Promethazine Hydrochloride Tablet
FDA Label NDC 65841-041

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 Promethazine Hydrochloride (NDC 65841-041). 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 65841-040-01 in bottle of 100 tablets

Promethazine Hydrochloride Tablets USP, 12.5 mg

Rx only

100 tablets

Promethzine Tablets, 12.5 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 02)

Promethzine Tablets, 12.5 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 02)

NDC 65841-041-01 in bottle of 100 tablets

Promethazine Hydrochloride Tablets USP, 25 mg

Rx only

100 tablets

Promethazine Tablets, 25 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 03)

Promethazine Tablets, 25 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 03)

NDC 65841-042-01 in bottle of 100 tablets

Promethazine Hydrochloride Tablets USP, 50 mg

Rx only

100 tablets

Promethazine Tablets, 50 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 04)

Promethazine Tablets, 50 mg (9ca44304 11ba 4e89 Bc90 10aaa8cf9fae 04)

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