Loxapine
Product Images NDC 10135-586

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Loxapine (NDC 10135-586). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Loxapine, A Dibenzoxazepine Compound, Represents A Subclass Of Tricyclic Antipsychotic Agents, Chemically Distinct From The Thioxanthenes, Butyrophenones, And Phenothiazines. Chemically, It Is 2-chloro-11-(4-methyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine. It Is Present As The Succinate Salt. (Loxapine Tablet 01)

Loxapine, A Dibenzoxazepine Compound, Represents A Subclass Of Tricyclic Antipsychotic Agents, Chemically Distinct From The Thioxanthenes, Butyrophenones, And Phenothiazines. Chemically, It Is 2-chloro-11-(4-methyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine. It Is Present As The Succinate Salt. (Loxapine Tablet 01)
Chemical structure of Loxapine base, depicting its fused ring system including a chlorinated aromatic ring and a methylated piperazine ring.*
FDA Label Image

Principal Display Panel Ndc 10135-0585-01marlexloxapinecapsules,usp5 mgrx Only100 Capsules (Loxapine Tablet 02)

Principal Display Panel Ndc 10135-0585-01marlexloxapinecapsules,usp5 mgrx Only100 Capsules (Loxapine Tablet 02)
Loxapine Capsules USP 5 mg label from Marlex Pharmaceuticals, Inc. The label indicates 100 capsules in the container. It includes storage instructions, a barcode, and details that Loxapine Succinate is the active ingredient. The product is manufactured by Lannett Company, Inc. and distributed by Marlex Pharmaceuticals, Inc.*
FDA Label Image

Principal Display Panel Ndc 10135-0586-01marlexloxapinecapsules,usp10 mgrx Only100 Capsules (Loxapine Tablet 03)

Principal Display Panel Ndc 10135-0586-01marlexloxapinecapsules,usp10 mgrx Only100 Capsules (Loxapine Tablet 03)
Label for Loxapine Capsules, USP 10 mg by Marlex Pharmaceuticals Inc. The label indicates 100 capsules per container, prescription only. It lists the active ingredient as Loxapine Succinate equivalent to 10 mg loxapine per capsule and several inactive ingredients. Storage instructions and dispensing requirements are included. Manufactured by Lannett Company, Inc. and distributed by Marlex Pharmaceuticals, Inc.*
FDA Label Image

Ndc 10135-0587-01marlexloxapinecapsules,usp25 mgrx Only100 Capsules (Loxapine Tablet 04)

Ndc 10135-0587-01marlexloxapinecapsules,usp25 mgrx Only100 Capsules (Loxapine Tablet 04)
Label for Loxapine Capsules, USP 25 mg by Marlex Pharmaceuticals Inc. The label includes dosage instructions, storage information, a barcode, and states the package contains 100 capsules. It lists inactive ingredients and specifies the product is manufactured by Lannett Company, Inc., Philadelphia, PA, and distributed by Marlex Pharmaceuticals, Inc., New Castle, DE.*
FDA Label Image

Principal Display Panel Ndc 10135-0588-01marlexloxapinecapsules,usp50 mgrx Only100 Capsules (Loxapine Tablet 05)

Principal Display Panel Ndc 10135-0588-01marlexloxapinecapsules,usp50 mgrx Only100 Capsules (Loxapine Tablet 05)
Label for Loxapine Capsules, USP 50 mg by Marlex Pharmaceuticals Inc. The label shows 100 capsules per container, with product storage instructions (20° to 25°C), and mentions dispensing in a child-resistant container. It lists inactive ingredients and states the product is manufactured by Lannett Company, Inc., Philadelphia, PA, and distributed by Marlex Pharmaceuticals, Inc., New Castle, DE. The label also includes an NDC barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.