Imipramine Hydrochloride Tablet, Film Coated
Product Images NDC 68180-313

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 Imipramine Hydrochloride (NDC 68180-313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

Imipramine Hydrochloride (Imipraminehydrochloride Figure 01)

Imipramine Hydrochloride (Imipraminehydrochloride Figure 01)
Chemical structure diagram of Imipramine Hydrochloride showing its molecular framework with associated hydrochloride component.*
FDA Label Image

Imi-10-100 (Imipraminehydrochloride Figure 02)

Imi-10-100 (Imipraminehydrochloride Figure 02)
Imipramine Hydrochloride Tablets USP 10 mg film-coated tablet label from Lupin Pharmaceuticals, Inc. The label includes dosage strength (10 mg), a note for pharmacists to dispense with medication guide separately, and packaging details specifying 100 tablets. Storage instructions and manufacturing information are also printed, along with a barcode and NDC number 68180-311-01.*
FDA Label Image

Imi-25-100 (Imipraminehydrochloride Figure 03)

Imi-25-100 (Imipraminehydrochloride Figure 03)
Imipramine Hydrochloride Tablets USP 25 mg film-coated tablet label from Lupin Pharmaceuticals, Inc. The label includes NDC 68180-312-01, storage instructions, dispensing warnings, and manufacturer information. The package contains 100 tablets in a 12 x 29 mm size.*
FDA Label Image

Imi-50-100 (Imipraminehydrochloride Figure 04)

Imi-50-100 (Imipraminehydrochloride Figure 04)
Package label for Imipramine Hydrochloride Tablets USP 50 mg film-coated tablets by Lupin Pharmaceuticals, Inc. The label shows the drug name, strength (50 mg), quantity (100 tablets), and instructions to dispense with medication guide. The label includes storage instructions, manufacturer information, NDC 68180-313-01, and a 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.