DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1USV Private Limited
03 1Chromo Laboratories India Private Limited
04 1Glaxo Wellcome Manufacturing Pte. Ltd
01 3Naratriptan Hydrochloride
02 1naratriptan hydrochloride
01 3India
02 1United Kingdom
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-085
Start Marketing Date : 2012-07-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62147-0195
Start Marketing Date : 2009-12-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-014
Start Marketing Date : 2021-06-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52482-011
Start Marketing Date : 2014-08-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Naratriptan Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naratriptan Hydrochloride, including repackagers and relabelers. The FDA regulates Naratriptan Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naratriptan 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 Naratriptan Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naratriptan Hydrochloride supplier is an individual or a company that provides Naratriptan Hydrochloride active pharmaceutical ingredient (API) or Naratriptan Hydrochloride finished formulations upon request. The Naratriptan Hydrochloride suppliers may include Naratriptan Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Naratriptan 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 Naratriptan Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naratriptan 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 Naratriptan 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 Naratriptan Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naratriptan Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naratriptan Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering Naratriptan Hydrochloride
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