Labetalol Hydrochloride Tablet, Film Coated
Product Images NDC 58657-602

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Labetalol Hydrochloride (NDC 58657-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Method Pharmaceuticals, 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

Desc (Desc)

Chemical structure of Labetalol Hydrochloride, showing its molecular components including phenyl and hydroxy groups, an amide functional group, and hydrochloride salt representation.*

FDA Label Image

100-100 (Label 2)

Label for Labetalol Hydrochloride Tablets, USP 100 mg, film-coated oral tablets. The label indicates a package of 100 tablets, Rx only, distributed by Method Pharmaceuticals, LLC in Southlake, TX. Additional label text includes storage instructions, child-resistant container information, and a barcode.*

FDA Label Image

100-500 (Label 5)

Label for Labetalol Hydrochloride Tablets USP 100 mg film-coated tablets, oral route. The package contains 500 tablets. Label displays NDC 58657-602-50 and identifies Method Pharmaceuticals, LLC as the labeler. Includes storage and safety instructions, and a barcode on the right side.*

FDA Label Image

200-100 (Label 3)

Label for Labetalol Hydrochloride Tablets, USP 200 mg film-coated tablets, oral use. This prescription drug package contains 100 tablets and is distributed by Method Pharmaceuticals, LLC. The label includes dosing information and storage instructions, along with the national drug code (NDC) 58657-603-01 and a barcode. The label prominently features the strength 200 mg in orange.*

FDA Label Image

1 (Label 6)

Label for Labetalol Hydrochloride Tablets, USP 200 mg oral film-coated tablets. Package contains 500 tablets. Labeler is Method Pharmaceuticals, LLC. The label includes dosage strength, count, NDC number 58657-603-50, and storage and handling instructions. It also states Rx Only and highlights no varnish on the label.*

FDA Label Image

4 (Label 4)

Label for Labetalol Hydrochloride Tablets USP 300 mg film-coated tablets by Method Pharmaceuticals. The label states Rx only and contains 100 tablets. Instructions for storage and usage are included along with a barcode. The label is white with green and black text and features the Method Pharmaceuticals logo.*

FDA Label Image

1 (Label 1)

Label for Labetalol Hydrochloride Tablets, USP, 300 mg film-coated oral tablets. The label indicates a 500-tablet package, labeled by Method Pharmaceuticals, LLC. The label features dosage and storage instructions, a barcode, and a marked "NO VARNISH" area.*

FDA Label Image

100mg (100mg Lab)

Label for Labetalol Hydrochloride 100 mg film-coated tablets, USP, unit dose packaging. The label indicates 100 tablets (10 x 10 unit-dose tablets), prescription only, distributed by Method Pharmaceuticals LLC, Southlake, TX. Storage instructions and usage warnings are included along with the NDC 58657-906-01.*

FDA Label Image

200 (200mg Lab)

Label for Labetalol Hydrochloride 200 mg film-coated tablets from Method Pharmaceuticals, LLC. The label states the drug is unit dose, prescription only, with a total of 100 tablets organized as 10 packs of 10 unit-dose tablets. Storage instructions specify 20° to 25°C and child-resistant packaging. It is intended for institutional use only.*

FDA Label Image

300 (300mg Lab)

Label for Labetalol Hydrochloride tablets, USP 300 mg, from Method Pharmaceuticals, LLC. The label indicates it is a unit dose package containing 100 tablets (10 x 10 unit-dose tablets). It includes dosage, storage instructions, and a barcode, noting prescription use only and a revision date of 10/2025.*

* 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.