Azithromycin Tablet, Film Coated
Product Images NDC 0527-2370

15 FDA label images from Lannett Company, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Azithromycin (NDC 0527-2370). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Chemical Structure (Azithromycin 01)

Chemical Structure (Azithromycin 01)
Chemical structure of azithromycin, showing its molecular framework with various methyl, hydroxyl, and nitrogen-containing groups arranged in a macrocyclic lactone ring with attached sugar moieties.*
FDA Label Image

Blister-250 (Blister250)

Blister-250 (Blister250)
Blister pack label for azithromycin tablet, USP 250 mg by Lannett Company, Inc. The label shows five individual tablet slots labeled Day 1 through Day 5, each with the tablet identification and barcode. Lot number and expiration date fields are present but not filled in.*
FDA Label Image

Blister-250-cr (Blister250cr)

Blister-250-cr (Blister250cr)
Label for Azithromycin Tablet USP 250 mg by Lannett Company, Inc. The label displays six individual tablets arranged with designated days (Day 1 to Day 5). Each section includes the product name, strength (250 mg), a barcode, and space for lot number and expiration date. The label is primarily pink with black text and barcode.*
FDA Label Image

Blister-500 (Blister500)

Blister-500 (Blister500)
Label for azithromycin tablets, USP 500 mg, film-coated, manufactured by Lannett Company, Inc. The label shows dosing for Day 1, Day 2, and Day 3, each with a barcode and space for lot and expiration information.*
FDA Label Image

Blister500cr (Blister500cr)

Blister500cr (Blister500cr)
Label for Azithromycin Tablet USP 500 mg oral film-coated tablets by Lannett Company, Inc. The label shows three daily dosing units labeled Day 1, Day 2, and Day 3. Each unit includes a barcode, lot number placeholder, expiration date placeholder, and the product name and strength in bold.*
FDA Label Image

Bottle-250 (Bottle250)

Bottle-250 (Bottle250)
Azithromycin Tablets, USP 250 mg film-coated tablets label for oral use. The label indicates the product contains azithromycin monohydrate equivalent to 250 mg azithromycin, with 30 tablets per package. Distributed by Lannett Company, Inc. and manufactured by Sunshine Lake Pharma Co., Ltd., Guangdong Province, China. Storage instructions specify 20° to 25°C.*
FDA Label Image

Bottle-500 (Bottle500)

Bottle-500 (Bottle500)
Azithromycin Tablets, USP 500 mg film-coated oral tablets in a container label. The label indicates a 30-tablet count, distributed by Lannett Company, Inc., Philadelphia, PA, and manufactured by Sunshine Lake Pharma Co., Ltd., Guangdong Province, China. Storage instructions specify 20° to 25°C controlled room temperature.*
FDA Label Image

Carton-250 (Carton250)

Carton-250 (Carton250)
Azithromycin 250 mg film-coated tablets packaging label from Lannett Company, Inc. The carton contains 1 card with 6 tablets. The label shows the proprietary name Azithromycin, strength 250 mg, dosage form as tablets USP, oral route, and prescribing information summary. It also includes instructions for use, storage recommendations, manufacturer details, and a barcode.*
FDA Label Image

Carton-500 (Carton500)

Carton-500 (Carton500)
Packaging label for Azithromycin Tablets, USP 500 mg by Lannett Company, Inc. The label indicates a single card containing 3 film-coated oral tablets. It includes dosing instructions for a full course of antibiotic therapy in 3 daily doses and storage recommendations at 20° to 25°C. The label also features a barcode and space for pharmacy labeling.*
FDA Label Image

Inner250cr (Inner250cr)

Inner250cr (Inner250cr)
Azithromycin 250 mg film-coated tablets carton label by Lannett Company, Inc. The label includes active ingredient and strength, prescription-only designation, package size (1 card x 6 tablets), storage instructions, and dosage summary. It also provides brief side effect and usage information and barcode with NDC 0527-2370-20. The product is oral human prescription drug.*
FDA Label Image

Inner500cr (Inner500cr)

Inner500cr (Inner500cr)
Azithromycin 500 mg film-coated tablets packaging label by Lannett Company, Inc. The label includes dosing information, indicating that each tablet contains azithromycin monohydrate equivalent to 500 mg of azithromycin, with a recommended course of 3 daily doses. The package contains 1 card with 3 tablets. It also provides storage instructions and common side effects, as well as manufacturer details showing production by Sunshine Lake Pharma Co., Ltd., China.*
FDA Label Image

Logo (Logo01)

FDA Label Image

Logo (Logo02)

FDA Label Image

Outer-carton-250-cr (Outer250cr)

Outer-carton-250-cr (Outer250cr)
Packaging label for Azithromycin tablets, USP, 250 mg film-coated oral tablets by Lannett Company, Inc. The label indicates prescription use, a 5-day full course antibiotic therapy, and contains dosing guidelines. The NDC 0527-2370-27 is shown on the label. The design features a white background with pink/red accents and includes barcode and distributor information.*
FDA Label Image

Outer500cr (Outer500cr)

Outer500cr (Outer500cr)
Azithromycin Tablets, USP 500 mg film-coated tablet packaging label from Lannett Company, Inc. The label includes NDC 0527-2395-22 and states the medication is for a full course of antibiotic therapy in 3 daily doses. The carton holds 3 cards of 3 tablets each. Storage, dosage, and distributor information are also visible on the label.*

* 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.