Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
01 1Olpha AS
02 1Cohance Lifesciences Limited
03 1Dr.Reddy's Laboratories Limited
04 1Anonima Materie Sintetiche and Affini (AMSA) Spa
05 4Chemo Biosynthesis s.r.l.
06 1Emcure Pharmaceuticals Limited
07 1HIKAL LIMITED
08 2Hainan Poly Pharm. Co., Ltd.
09 1Hetero Drugs Limited
10 3Industriale Chimica s.r.l.
11 1Lundbeck Pharmaceuticals Italy S.p.A.
12 1MSN Pharmachem Private Limited
13 2MYLAN LABORATORIES LIMITED
14 1Megafine Pharma (P) Limited
15 2Olon SpA
16 1Optimus Drugs Private Limited
17 2PROCOS S.p.A.
18 1SICOR Societa' Italiana Corticosteroidi s.r.l.
19 1Siegfried Evionnaz SA
20 1Tianish Laboratories Private Limited
21 1Unichem Laboratories Limited, India
22 1Uquifa Spain
01 7MEMANTINE HYDROCHLORIDE
02 2Memantine
03 1Memantine Base
04 1Memantine HCl
05 20Memantine Hydrochloride
01 2China
02 1Denmark
03 10India
04 9Italy
05 1Latvia
06 5Spain
07 1Switzerland
08 2U.S.A
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
NDC Package Code : 63818-0004
Start Marketing Date : 2016-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
NDC Package Code : 76072-1004
Start Marketing Date : 2016-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-860
Start Marketing Date : 2010-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17373-1146
Start Marketing Date : 2017-01-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 14593-870
Start Marketing Date : 2023-12-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14335-160
Start Marketing Date : 2022-11-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 14335-160
Start Marketing Date : 2021-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0025
Start Marketing Date : 2006-01-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0076
Start Marketing Date : 2017-02-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17381-260
Start Marketing Date : 2010-04-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Namenda manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Namenda, including repackagers and relabelers. The FDA regulates Namenda manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Namenda 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 Namenda manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Namenda supplier is an individual or a company that provides Namenda active pharmaceutical ingredient (API) or Namenda finished formulations upon request. The Namenda suppliers may include Namenda API manufacturers, exporters, distributors and traders.
click here to find a list of Namenda 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 Namenda as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Namenda 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 Namenda 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 Namenda and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Namenda NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Namenda suppliers with NDC on PharmaCompass.
We have 22 companies offering Namenda
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
