FDA Label for Mirtazapine
View Indications, Usage & Precautions
Mirtazapine Product Label
The following document was submitted to the FDA by the labeler of this product Square Pharmaceuticals 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 76483-110-00 in unit-dose blister cartons of 30 (5 x 6 blisters) Unit-of-use Tablets
Mirtazapine Orally Disintegrating Tablets USP, 15 mg
Rx only
30 Tablets
NDC 76483-111-00 in unit-dose blister cartons of 30 (5 x 6 blisters) Unit-of-use Tablets
Mirtazapine Orally Disintegrating Tablets USP, 30 mg
Rx only
30 Tablets
NDC 76483-112-00 in unit-dose blister cartons of 30 (5 x 6 blisters) Unit-of-use Tablets
Mirtazapine Orally Disintegrating Tablets USP, 45 mg
Rx only
30 Tablets
* Please review the disclaimer below.