Ropinirole Hydrochloride
Product Images NDC 64220-421

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 64220-421). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Huahai Pharmaceutical Co., Ltd., 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

Structural Formula Of Ropinirole HCl (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 01)

FDA Label Image

Ropinirole HCl 0.25mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 05)

Ropinirole HCl 0.25mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 05)
This is a product description for Ropinirole Hydrochloride Tablets. Each tablet contains 0.25mg of ropinirole hydrochloride. The usual dosage can be found in the accompanying prescribing information. The tablets should be stored at room temperature and protected from light and moisture. Safety closures should be used when dispensing the product, and it should be kept out of reach of children. The drug is manufactured by Zhejiang Huahai Pharmaceutical Co. in China and distributed by Prinston Pharmaceutical Inc. in Cranbury, NJ, USA. The LOT and EXP are not available.*
FDA Label Image

Ropinirole HCl 0.5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 06)

Ropinirole HCl 0.5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 06)
This is a description of a prescription drug called rOPINIRole Hydrochloride Tablets, with the NDC code 64220-421-01. Each tablet contains 0.5 mg of ropinirole hydrochloride. It is advised to dispense the Patient Information Leaflet to each patient. Safety closures should be used when dispensing the product. The drug should be stored at a temperature between 20° to 25°C, protected from light and moisture. The manufacturer is Zhejiang Huahai Pharmaceutical Co. and the distributor is Prinston Pharmaceutical Inc. It is important to keep this drug out of reach of children. The lot number and expiration date are not provided in the text.*
FDA Label Image

Ropinirole HCl 1mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 07)

Ropinirole HCl 1mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 07)
This is a description of a medication with the National Drug Code (NDC) of 64220-422-01. The medication is called rOPINIRole. It comes in tablet form, and each tablet contains 1 mg of ropinirole hydrochloride. The medication is typically prescribed, and a pharmacist should provide the patient with a leaflet detailing the medication's use. The medication should be kept at room temperature and protected from light and moisture. The closure safety mechanisms should be used to dispense the product unless a physician directs otherwise. The manufacturer is Zhejiang Huahai Pharmaceutical Co., Ltd., and the medication is sold through Prinston Pharmaceutical Inc. in Cranbury, NJ.*
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Ropinirole HCl 2mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 08)

Ropinirole HCl 2mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 08)
This is a prescription drug with NDC 64220-423-01. It contains 100 tablets of rOPINIRole Hydrochloride, with each tablet having 2mg ropinirole hydrochloride. Patients should be given the patient information leaflet with the drug. The drug should be stored at 20° to 25°C and protected from light and moisture. The product should be kept out of the reach of children. The drug is manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd. and marketed by Prinston Pharmaceutical Inc. It is meant to be prescribed by a physician.*
FDA Label Image

Ropinirole HCl 3mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 09)

Ropinirole HCl 3mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 09)
NDC 64220-424-01 is a prescription drug used to treat symptoms of Restless Legs Syndrome. It is available in tablet form and contains ropinirole hydrochloride equivalent to ropinirole base 3 mg. It is recommended to store the tablets at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. It is important to use safety closures when dispensing this product unless otherwise directed by the physician or requested by the purchaser. This drug should be kept out of the reach of children. The manufacturer is Zhejiang Huahai Pharmaceutical Co., Ltd. Linhai, Zhejiang, China 317024, and the distributor is Prinston Pharmaceutical Inc. Cranbury, NJ, USA 08512.*
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Ropinirole HCl 4mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 10)

Ropinirole HCl 4mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 10)
This is a medication called Ropinirole Hydrochloride, which comes in tablet form with each tablet containing 4mg of Ropinirole. It is usually prescribed for a certain medical condition. The medication should be stored at room temperature and away from direct light and moisture. The manufacturer is Zhejiang Huahai Pharmaceutical Co. Ltd., located in Linhai, Zhejiang, China. Prinston Pharmaceutical Inc., based in Cranbury, NJ, USA, distributes the medication. It is important to keep the medication out of the reach of children and use safety closures when dispensing. The packaging includes 100 tablets with a prescription required for purchase. A pharmacist is requested to provide a patient information leaflet with each package.*
FDA Label Image

Ropinirole HCl 5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 11)

Ropinirole HCl 5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 11)
This is a description for ROPINIRole Hydrochloride Tablets, with each tablet containing Ropinirole hydrochloride equivalent to ropinirole base 5 mg. It is recommended to store these tablets at 20° to 25°C (68° to 77°F) and protect from light and moisture. Ensure safety closures when dispensing the product, unless directed otherwise by a physician. This drug is only available through prescription and a Patient Information Leaflet must be provided with each dose. It is manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd, Linhai, Zhejiang, China and is distributed by Prinston Pharmaceutical Inc, Cranbury, NJ, USA 08512. Expiry date and lot number should be checked before use.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.