Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1PCAS FINLAND
02 1Medichem S.A.
03 2USV Private Limited
04 1Curia Spain S.A.U.
05 2F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
06 1F.I.S. Fabbrica Italiana Sintetici S.P.A.
07 1FDC Limited
08 1Glenmark Life Sciences Limited
09 1Indoco Remedies Limited
10 1Kyowa Pharma Chemical Co., Ltd.
11 1MSN Laboratories Private Limited
12 1Urquima, S.A.
01 1OLOPATADINE HCL
02 3OLOPATADINE HYDROCHLORIDE
03 1Olopatadine HCl
04 8Olopatadine Hydrochloride
05 1olopatadine hydrochloride
01 1France
02 6India
03 3Italy
04 1Japan
05 2Spain
06 1U.S.A
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 51014-7733
Start Marketing Date : 2010-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 53296-0078
Start Marketing Date : 2010-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0117
Start Marketing Date : 2009-12-04
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 : 62147-0118
Start Marketing Date : 2009-12-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0100
Start Marketing Date : 2011-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0165
Start Marketing Date : 2023-09-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52133-0036
Start Marketing Date : 1996-12-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14445-009
Start Marketing Date : 2013-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12079-2002
Start Marketing Date : 2013-10-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0050
Start Marketing Date : 2010-03-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Olopatadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Olopatadine Hydrochloride, including repackagers and relabelers. The FDA regulates Olopatadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Olopatadine 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 Olopatadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Olopatadine Hydrochloride supplier is an individual or a company that provides Olopatadine Hydrochloride active pharmaceutical ingredient (API) or Olopatadine Hydrochloride finished formulations upon request. The Olopatadine Hydrochloride suppliers may include Olopatadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Olopatadine 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 Olopatadine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Olopatadine 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 Olopatadine 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 Olopatadine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Olopatadine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Olopatadine Hydrochloride suppliers with NDC on PharmaCompass.
We have 11 companies offering Olopatadine Hydrochloride
Get in contact with the supplier of your choice:
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