01 1AX Pharmaceutical Corp
02 1American Pacific Corporation
03 1Azico Biophore India Private Limited
04 1BrightGene Bio-Medical Technology Co., Ltd.
05 1Chromo Laboratories India Private Limited
06 1Cipla Ltd.
07 1Dasami Lab Private Limited
08 1Hetero Labs Limited
09 1Hubei Gedian humanwell Pharmaceutical Co., Ltd
10 1MSN Life Sciences Private Limited
11 1MSN Pharmachem Private Limited
12 1MYLAN LABORATORIES LIMITED
13 1PATHEON API, INC
14 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
15 1Shanghai Desano Chemical Pharmaceutical Co., Ltd.
16 1Tianish Laboratories Private Limited
01 14Oseltamivir Phosphate
02 1Oseltamivir phosphate
03 1oseltamivir phosphate
01 1Canada
02 3China
03 9India
04 3U.S.A
NDC Package Code : 50683-0557
Start Marketing Date : 2021-04-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62227-026
Start Marketing Date : 2024-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-025
Start Marketing Date : 2022-04-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7739
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0029
Start Marketing Date : 2007-07-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51508-018
Start Marketing Date : 2024-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0028
Start Marketing Date : 2011-12-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63482-799
Start Marketing Date : 1999-10-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42931-089
Start Marketing Date : 2022-02-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-871
Start Marketing Date : 2017-10-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oseltamivir Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oseltamivir Phosphate, including repackagers and relabelers. The FDA regulates Oseltamivir Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oseltamivir Phosphate 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 Oseltamivir Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oseltamivir Phosphate supplier is an individual or a company that provides Oseltamivir Phosphate active pharmaceutical ingredient (API) or Oseltamivir Phosphate finished formulations upon request. The Oseltamivir Phosphate suppliers may include Oseltamivir Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Oseltamivir Phosphate 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 Oseltamivir Phosphate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oseltamivir Phosphate 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 Oseltamivir Phosphate 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 Oseltamivir Phosphate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oseltamivir Phosphate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oseltamivir Phosphate suppliers with NDC on PharmaCompass.
We have 15 companies offering Oseltamivir Phosphate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
