DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Neuland Laboratories Limited
03 2USV Private Limited
04 1Glenmark Life Sciences Limited
05 1Synthimed Labs Private Limited
06 1Urquima, S.A.
07 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
08 1Zhejiang Huahai Pharmaceutical Co., LTD
01 1Ropinirole 5% w/w Triturate with Lactose
02 8Ropinirole Hydrochloride
01 2China
02 6India
03 1Spain
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-091
Start Marketing Date : 2010-02-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-0133
Start Marketing Date : 2017-12-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0008
Start Marketing Date : 2010-02-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0015
Start Marketing Date : 2010-01-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-853
Start Marketing Date : 2007-06-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65096-0102
Start Marketing Date : 2013-07-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54752-0005
Start Marketing Date : 1997-09-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-993
Start Marketing Date : 2021-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.0057kg/.1kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 64220-121
Start Marketing Date : 2011-02-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ropinirole Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ropinirole Hydrochloride, including repackagers and relabelers. The FDA regulates Ropinirole Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ropinirole Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Ropinirole Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ropinirole Hydrochloride supplier is an individual or a company that provides Ropinirole Hydrochloride active pharmaceutical ingredient (API) or Ropinirole Hydrochloride finished formulations upon request. The Ropinirole Hydrochloride suppliers may include Ropinirole Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ropinirole Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Ropinirole Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ropinirole Hydrochloride API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Ropinirole Hydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Ropinirole Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ropinirole Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ropinirole Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Ropinirole Hydrochloride
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