Loxapine Capsule
Product Images NDC 70518-0416

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Loxapine (NDC 70518-0416). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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 50mg 70518 0416 00

Loxapine 50mg 70518 0416 00
Loxapine is a medication available in a capsule form with 50mg strength. A bottle contains 30 capsules, and it is an RX medication that must be kept out of children's reach. The label provides lot number information and source NDC. It is manufactured by Actavis in Sunrise, Florida. The medication must be stored between 20-25°C (58-77°F), with excursions allowed to 15-30°C (59-86°F), and RemedyRepack Inc. repackaged it in Indiana, PA 15701. The package insert can assist with directions for use.*
FDA Label Image

Loxapine 50mg 70518 0416 01

Loxapine 50mg 70518 0416 01
Loxapine is a prescription medication that comes in a capsule form of 50 mg, with 100 capsules per bottle. The product has a National Drug Code (NDC) of 70518-0416-01 5 and an expiration date that is not available. It was manufactured by Actavis located in Sunrise, FL 33325, and the source NDC is 00591-0372-01. It is mandatory to keep this medication out of the reach of children. Directions for use can be found in the package insert. The product must be stored at 20-25°C [58-77°F) with excursions allowed to 15-30°C (59-86°F) [See USP]. The product was repackaged by RemedyRepack Inc. located in Indiana, PA 15701, and can be contacted at 724.455.8762.*
FDA Label Image

Loxapine 50mg 70518 0416 02

Loxapine 50mg 70518 0416 02
Loxapine is a medication available in the form of 50 mg capsule for prescription use only. The NDC number for this medicine is 70518-0416-02, and the LOT number is not available. The expiration and source of this medication can be found on the packaging insert, and the manufacturer is Actavis in Sunrise, FL. The medication should be stored between 20-25°C (58-77°F) with the excursions permitted to 15-30°C (59-86°F) and kept away from the reach of children. For directions of use, refer to the Package Insert. This medication is repackaged by RemedyRepack Inc. in Indiana, PA 15701.*
FDA Label Image

Image 1

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.