01 1Cambrex Profarmaco Milano Srl
02 1Cipla Ltd.
03 1LETCO MEDICAL, LLC
04 1Melody Healthcare Pvt. Ltd.
05 1Professional Compounding Centers of America dba PCCA
06 1Spectrum Laboratory Products, Inc.
01 2TERBUTALINE SULFATE
02 4Terbutaline Sulfate
01 2India
02 3U.S.A
03 1United Kingdom
NDC Package Code : 12828-0053
Start Marketing Date : 1998-08-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7513
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 : 62991-1152
Start Marketing Date : 2012-01-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 69826-0001
Start Marketing Date : 2018-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2765
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-7631
Start Marketing Date : 1996-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Terbutaline Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terbutaline Sulfate, including repackagers and relabelers. The FDA regulates Terbutaline Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terbutaline Sulfate 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 Terbutaline Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terbutaline Sulfate supplier is an individual or a company that provides Terbutaline Sulfate active pharmaceutical ingredient (API) or Terbutaline Sulfate finished formulations upon request. The Terbutaline Sulfate suppliers may include Terbutaline Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Terbutaline Sulfate 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 Terbutaline Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Terbutaline Sulfate 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 Terbutaline Sulfate 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 Terbutaline Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Terbutaline Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Terbutaline Sulfate suppliers with NDC on PharmaCompass.
We have 6 companies offering Terbutaline Sulfate
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