Isosorbide Dinitrate Tablet
Product Images NDC 49884-021

9 FDA label images from Par Health Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Isosorbide Dinitrate (NDC 49884-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Par Health Usa, 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

This Is The Structural Formula (Isosorbide Dinitrate 1)

This Is The Structural Formula (Isosorbide Dinitrate 1)
Chemical structure of isosorbide dinitrate, showing the arrangement of carbon, hydrogen, and nitrate groups in the molecule as depicted in the diagram.*
FDA Label Image

5mg-100s (Isosorbide Dinitrate 2)

5mg-100s (Isosorbide Dinitrate 2)
Label for Isosorbide Dinitrate Tablets USP, 5 mg oral tablets, packaged as 100 tablets. The label includes dosage strength, manufacturer Par Pharmaceutical, and storage instructions. The label shows the NDC 49884-020-01 and states Rx only.*
FDA Label Image

10mg-100s (Isosorbide Dinitrate 3)

10mg-100s (Isosorbide Dinitrate 3)
Label for Isosorbide Dinitrate Tablets USP oral 10 mg by Par Pharmaceutical. The label indicates a package of 100 tablets, prescription only. It includes storage instructions, dosage note, and warnings to keep out of reach of children. The label shows a barcode and manufacturer details.*
FDA Label Image

20mg-100s (Isosorbide Dinitrate 4)

20mg-100s (Isosorbide Dinitrate 4)
Label for Isosorbide Dinitrate Tablets, USP, oral dosage form, 10 mg strength. The label states the product contains 100 tablets, is Rx only, and is manufactured by Par Pharmaceutical. Instructions note the tablet contains 10 mg isosorbide dinitrate and advise to read accompanying literature for dosage and keep out of reach of children. Storage instructions recommend room temperature around 25°C (77°F), protection from light, and keeping the bottle tightly closed.*
FDA Label Image

30mg-100s (Isosorbide Dinitrate 5)

30mg-100s (Isosorbide Dinitrate 5)
Label for Isosorbide Dinitrate Tablets, USP 10 mg oral tablets, manufactured by Par Pharmaceutical. The label indicates a quantity of 100 tablets per bottle, prescription only. It includes dosing information, storage instructions, and distributor and manufacturer details, alongside a barcode and NDC number 49884-021-01.*
FDA Label Image

Isosorbide Dinitrate 6

Isosorbide Dinitrate 6
Label for Isosorbide Dinitrate Tablets, USP 20 mg oral tablets, packaged as 100 tablets. The label indicates the product is prescription-only, manufactured by Par Health USA, LLC, and includes usage directions and storage instructions on the packaging.*
FDA Label Image

Isosorbide Dinitrate 7

Isosorbide Dinitrate 7
Label for Isosorbide Dinitrate Tablets USP 20 mg oral tablets. The label indicates a bottle containing 100 tablets, labeled Rx only, manufactured and distributed by Par Health USA, LLC. Additional storage instructions and drug information such as dosage, container type, and safety warnings are also visible.*
FDA Label Image

Isosorbide Dinitrate 8

Isosorbide Dinitrate 8
Isosorbide Dinitrate Tablets USP oral tablets, 30 mg strength, in a 100 count package. Label includes dosage information, storage instructions, and is marked Rx only. Manufactured by Par Pharmaceuticals, with barcode and NDC 49884-009-01.*
FDA Label Image

Isosorbide Dinitrate 9

Isosorbide Dinitrate 9
Label for Isosorbide Dinitrate Tablets USP, oral, 30 mg strength, supplied in a bottle containing 100 tablets. The label includes dosage instructions, storage conditions, and manufacturer information. Labeler is Par Health USA, LLC.*

* 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.