Pramipexole Dihydrochloride Tablet
Product Images NDC 50228-126

13 FDA label images from Sciegen Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 50228-126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen 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

Pramipexol-fig10 (Pramipexol Fig10)

Pramipexol-fig10 (Pramipexol Fig10)
Label for Pramipexole Dihydrochloride 1 mg tablets by ScieGen Pharmaceuticals Inc. The label indicates 90 tablets per container, with prescription only. It includes storage instructions, dosage strength, and a barcode. The label is in English and states to keep medication out of reach of children.*
FDA Label Image

Pramipexol-fig11 (Pramipexol Fig11)

Pramipexol-fig11 (Pramipexol Fig11)
Pramipexole Dihydrochloride Tablets 1 mg oral dosage form by ScieGen Pharmaceuticals Inc. The label states the package contains 1000 tablets, with instructions to dispense accompanying patient information. It includes storage conditions (20° to 25°C), dosage form, and a warning to keep medication out of reach of children. A barcode and NDC 50228-130-10 are visible.*
FDA Label Image

Pramipexol-fig12 (Pramipexol Fig12)

Pramipexol-fig12 (Pramipexol Fig12)
Label for Pramipexole Dihydrochloride tablets, 1.5 mg strength, manufactured by ScieGen Pharmaceuticals Inc. The label includes the NDC 50228-131-90 and indicates a package of 90 tablets for oral use. Storage instructions specify 20° to 25°C (68° to 77°F), protection from light, and use of a tight, light-resistant, and child-resistant container. The label advises pharmacists to dispense accompanying patient information.*
FDA Label Image

Pramipexol-fig13 (Pramipexol Fig13)

Pramipexol-fig13 (Pramipexol Fig13)
Pramipexole Dihydrochloride 1.5 mg tablets label from ScieGen Pharmaceuticals, containing 1000 tablets. The label includes dosage strength, drug name, storage instructions, and a barcode for product identification.*
FDA Label Image

Pramipexol-fig2 (Pramipexol Fig2)

Pramipexol-fig2 (Pramipexol Fig2)
Pramipexole Dihydrochloride 0.125 mg tablets label from ScieGen Pharmaceuticals Inc. The label states the strength as 0.125 mg per tablet and includes storage instructions and dispensing information. The package contains 90 tablets, designated for prescription use only.*
FDA Label Image

Pramipexol-fig3 (Pramipexol Fig3)

Pramipexol-fig3 (Pramipexol Fig3)
Label for Pramipexole Dihydrochloride tablets, 0.125 mg strength, manufactured by ScieGen Pharmaceuticals Inc. The label shows dosage form as tablets, with a package size of 1000 tablets. It includes storage instructions, pharmacist dispensing directions, and a barcode. The label indicates prescription use only.*
FDA Label Image

Pramipexol-fig4 (Pramipexol Fig4)

Pramipexol-fig4 (Pramipexol Fig4)
Label for Pramipexole Dihydrochloride 0.25 mg oral tablets by ScieGen Pharmaceuticals Inc. The label indicates 90 tablets per container with prescription-only status. It includes storage instructions, dosage advisory to read prescribing information, and manufacturer details. The NDC code 50228-127-90 and a barcode are also visible.*
FDA Label Image

Pramipexol-fig5 (Pramipexol Fig5)

Pramipexol-fig5 (Pramipexol Fig5)
Label for Pramipexole Dihydrochloride tablets, 0.25 mg oral dosage form, manufactured by ScieGen Pharmaceuticals Inc. The package contains 1000 tablets. Instructions mention dispensing accompanying patient information and storage at controlled room temperature, protected from light. The label includes the NDC 50228-127-10 and a barcode.*
FDA Label Image

Pramipexol-fig6 (Pramipexol Fig6)

Pramipexol-fig6 (Pramipexol Fig6)
Pramipexole Dihydrochloride Tablets 0.5 mg oral dosage form label. The label indicates the product contains 90 tablets, is manufactured by ScieGen Pharmaceuticals Inc., and includes storage instructions and a barcode. It is a prescription-only medication.*
FDA Label Image

Pramipexol-fig7 (Pramipexol Fig7)

Pramipexol-fig7 (Pramipexol Fig7)
Label for Pramipexole Dihydrochloride 0.5 mg oral tablets by ScieGen Pharmaceuticals Inc. The label states the active ingredient strength, storage instructions, and quantity of 1000 tablets. It includes the NDC 50228-128-10, pharmacist dispensing information, and warnings to keep medication out of children's reach. The label emphasizes prescription use only.*
FDA Label Image

Pramipexol-fig8 (Pramipexol Fig8)

Pramipexol-fig8 (Pramipexol Fig8)
Label for Pramipexole Dihydrochloride Tablets 0.75 mg by ScieGen Pharmaceuticals Inc. The label includes dosage details, storage instructions, quantity of 90 tablets, and a barcode. It also notes prescription status with 'Rx Only' and advises dispensing patient information.*
FDA Label Image

Pramipexol-fig9 (Pramipexol Fig9)

Pramipexol-fig9 (Pramipexol Fig9)
Label for Pramipexole Dihydrochloride tablets, 0.75 mg strength, manufactured by ScieGen Pharmaceuticals Inc. The label includes the NDC 50228-129-10, dosage form as tablets, quantity of 1000 tablets, and storage instructions. It features a barcode and highlights that the product is Rx only with a note for pharmacist dispensing information.*
FDA Label Image

Structural Formula (Pramipexol Str)

Structural Formula (Pramipexol Str)
Chemical structure of Pramipexole Dihydrochloride, showing its molecular composition including a bicyclic ring system with nitrogen and sulfur atoms, an amine group, and two hydrochloride and one water molecules as indicated.*

* 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.