Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 2Bayer AG
03 1Cipla Ltd.
04 1Curia Spain S.A.U.
05 1Formosa Laboratories, Inc.
06 2Gedeon Richter Plc.
07 2Hubei Gedian humanwell Pharmaceutical Co., Ltd
08 3Industriale Chimica s.r.l.
09 2Qinhuangdao Zizhu Pharmaceutical Co., Ltd.
10 2STERLING SPA
11 1ScinoPharm Taiwan Ltd.
12 2Sterling Chemical Malta Ltd
01 4LEVONORGESTREL
02 1LEVONORGESTREL ACETATE
03 12Levonorgestrel
04 1NORGESTREL
05 2Norgestrel
01 4China
02 2Germany
03 2Hungary
04 2India
05 5Italy
06 2Malta
07 2Taiwan
08 1U.S.A
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0047
Start Marketing Date : 2017-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12866-1010
Start Marketing Date : 2017-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12866-1011
Start Marketing Date : 2017-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7669
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 : 45541-1149
Start Marketing Date : 2001-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45541-1174
Start Marketing Date : 1995-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51508-203
Start Marketing Date : 2024-11-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51508-012
Start Marketing Date : 2022-03-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44132-004
Start Marketing Date : 2012-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 44132-012
Start Marketing Date : 2014-06-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A (-)-Norgestrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (-)-Norgestrel, including repackagers and relabelers. The FDA regulates (-)-Norgestrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (-)-Norgestrel 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 (-)-Norgestrel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (-)-Norgestrel supplier is an individual or a company that provides (-)-Norgestrel active pharmaceutical ingredient (API) or (-)-Norgestrel finished formulations upon request. The (-)-Norgestrel suppliers may include (-)-Norgestrel API manufacturers, exporters, distributors and traders.
click here to find a list of (-)-Norgestrel 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 (-)-Norgestrel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for (-)-Norgestrel 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 (-)-Norgestrel 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 (-)-Norgestrel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a (-)-Norgestrel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of (-)-Norgestrel suppliers with NDC on PharmaCompass.
We have 12 companies offering (-)-Norgestrel
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