Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 62175-261

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 62175-261). 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 (Nifedipine Extended Release Tablets Usp 1)

Chemical structure diagram of Nifedipine, showing its molecular framework with substituent groups including methyl, nitro, and ester functionalities.*

FDA Label Image

Nifedipine 90mg 90ct (Nifedipine Extended Release Tablets Usp 10)

Label for Nifedipine Extended-release Tablets, USP, 90 mg by Lannett Company, Inc. The label includes dosage strength (90 mg), quantity (100 tablets), storage instructions (20°-25°C), dosage note to see package insert, and a warning to keep out of reach of children. The label also indicates prescription use only (Rx Only) and displays a barcode.*

FDA Label Image

Logo (Nifedipine Extended Release Tablets Usp 2)

Nifedipine 30 mg extended-release tablets, USP, film-coated oral tablets distributed by Lannett Company, Inc. The label specifies 90 tablets per container, with storage instructions and dosing notes. The NDC number is 62175-260-46.*

FDA Label Image

Nifedipine 30 mg 90ct (Nifedipine Extended Release Tablets Usp 3)

Label for Nifedipine Extended-release Tablets, USP, 30 mg strength, film-coated extended-release oral tablets. The label shows that each tablet contains 33 mg nifedipine to deliver a 30 mg dose. The package contains 100 tablets and is distributed by Lannett Company, Inc., Philadelphia, PA.*

FDA Label Image

Nifedipine Er 30 mg 100ct (Nifedipine Extended Release Tablets Usp 4)

Label for Nifedipine extended-release tablets, USP, 30 mg strength. The label states the product contains 300 film-coated tablets for oral use. It includes storage instructions, dosage notes, and a warning to keep out of reach of children. The product is distributed by Lannett Company, Inc.*

FDA Label Image

Nifedipine 30mg 300ct (Nifedipine Extended Release Tablets Usp 5)

Label for Nifedipine Extended-release Tablets, USP, 60 mg strength. The label indicates a supply of 90 film-coated extended-release tablets for oral use. The product is distributed by Lannett Company, Inc., Philadelphia, PA. Storage instructions and warnings are included on the label.*

FDA Label Image

Nifedipine 60mg 90ct (Nifedipine Extended Release Tablets Usp 6)

Label for Nifedipine Extended-release Tablets, USP, showing a 60 mg strength. The label indicates 100 tablets per container by Lannett Company, Inc. It includes storage instructions, dosage reference to the package insert, and a barcode. The product is for oral use and prescription only.*

FDA Label Image

Nifedipine 60mg 100ct (Nifedipine Extended Release Tablets Usp 7)

Label for Nifedipine Extended-release Tablets USP 60 mg by Lannett Company, Inc. The film-coated tablets are oral dosage form, with 300 tablets per container. The label includes dosing instruction to see package insert, storage conditions, and warnings about moisture and child safety. The label also shows the NDC 62175-261-55 and barcode.*

FDA Label Image

Nifedipine 60mg 300ct (Nifedipine Extended Release Tablets Usp 8)

Label for Nifedipine Extended-release Tablets, USP showing 90 mg strength. The label includes the NDC number 62175-262-32, indicates the product contains 30 tablets, and states it is for prescription use only. Manufacturer is Lannett Company, Inc. The label also provides storage instructions, dosage reference to package insert, and a warning to keep out of reach of children.*

FDA Label Image

Nifedipine 90mg 30ct (Nifedipine Extended Release Tablets Usp 9)

Nifedipine Extended-release Tablets, USP 90 mg film-coated tablets in a container of 90 tablets by Lannett Company, Inc. The label indicates storage instructions, dosage reference, and a warning to keep out of reach of children. The NDC number 62175-262-46 appears on the label along with the 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.