FDA Label for Paroxetine

View Indications, Usage & Precautions

Paroxetine Product Label

The following document was submitted to the FDA by the labeler of this product Zydus Lifesciences Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Package Label.Principal Display Panel



NDC 65841-097-05 in pack count of 500 tablets

Paroxetine Tablets USP, 10 mg

Rx only

500 tablets

NDC 65841-098-16 in pack count of 90 tablets

Paroxetine Tablets USP, 20 mg

Rx only

90 tablets

NDC 65841-099-10 in pack count of 1000 tablets

Paroxetine Tablets USP, 30 mg

Rx only

1000 tablets

NDC 65841-601-06 in pack count of 30 tablets

Paroxetine Tablets USP, 40 mg

Rx only

30 tablets


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