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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