Methylphenidate Hydrochloride Tablet
Product Images NDC 67877-617

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Methylphenidate Hydrochloride (NDC 67877-617). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, 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

Methylphenidate-structure (Methylphenidate Structure)

FDA Label Image

Methylphenidate 10mg 100s 1

This is a medication label for tablets containing 10mg of Methylphenidate Hydrochloride with instructions on storage conditions and cautionary notes. The manufacturer is listed as Ao Laboratories and the label should only be dispensed with an attached medication guide. There is a mention of a recommended storage temperature range.*

FDA Label Image

Methylphenidate 10mg 10s 1

This is a medication called Methylphenidate Hydrochloride Tablets, USP. It is a package of 10 tablets that must be dispensed with a medication guide attached or provided separately. The package is not child resistant. Each tablet contains 10 mg of MoybrerdaloHyrochasd, USP. The dosage of the medication should be followed as outlined in the package insert. It should be stored at a temperature between 20°C to 25°C, with excursions permitted between 10°C to 30°C. The medication should be protected from light. The manufacturer is A Laborares and it is distributed by Ascend Laboratories LLC. No further information is given.*

FDA Label Image

Methylphenidate 20mg 100s 1

This is a description for a medication called Methylphenidate Hydrochloride Tablets. It comes in a pack of 100 tablets with the NDC number 67877-618.01 and is only available with a prescription. The tablets should be protected from light and should be dispensed with the medication guide attached or provided separately. The label includes the lot number V6 and the dimensions of the unvarnished area of the label. The rest of the label should be coated with UV Varnish. The location of the manufacturer is Parsippany, New Jersey.*

FDA Label Image

Methylphenidate 20mg 10s 1

This is a package of Methylphenidate Hydrochloride Tablets, USP. It contains 10 tablets in a unit-dose package that is not child resistant. It is required to dispense the medication with the attached or provided Medication Guide. Each tablet contains 20 Mg of Methylphenidate Hydrochloride, USP. The dosage information is included within the package insert which should be stored at a temperature between 20°C to 25°C (68°F to 77°F). The manufacturer is A Laboratories located in Fenton, MO, and it is distributed by Ascend Laboratories, LLC in Parsippany, NJ.*

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Methylphenidate 5mg 100s 1

Each tablet contains Methylphenidate Hydrochloride, a medication commonly used to treat ADHD. The product is accompanied by a Medication Guide and should be stored within the temperature range of 20°C to 25°C (66°F to 77°F), with excursions permitted to 15°C to 30°C (59°F to 86°F). The tablets are provided by Akem Laboratories and distributed by Ascend Laboratories LLC. Dosage and usage instructions are available on the package insert.*

FDA Label Image

Methylphenidate 5mg 10s 1

This is a description of Methylphenidate Hydrochloride Tablets, USP, a prescription medication used to treat ADHD and narcolepsy. The tablets are not child-resistant, and are packaged in a unit-dose package containing 10 tablets. The medication guide is attached to the package or provided separately. The dosage of the medication is not available from this text, but it should be seen from the package insert. The manufacturer of the medication is Alam Laboratories while the distributor is ASCEND.*

* 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.