01 1Catalent Micron Technologies, Inc.
02 1Unichem Laboratories Limited, India
01 2Bendroflumethiazide
01 1India
02 1U.S.A
NDC Package Code : 69988-0028
Start Marketing Date : 2008-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 53747-004
Start Marketing Date : 2002-02-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Berk Brand of Bendroflumethiazide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Berk Brand of Bendroflumethiazide, including repackagers and relabelers. The FDA regulates Berk Brand of Bendroflumethiazide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Berk Brand of Bendroflumethiazide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Berk Brand of Bendroflumethiazide supplier is an individual or a company that provides Berk Brand of Bendroflumethiazide active pharmaceutical ingredient (API) or Berk Brand of Bendroflumethiazide finished formulations upon request. The Berk Brand of Bendroflumethiazide suppliers may include Berk Brand of Bendroflumethiazide API manufacturers, exporters, distributors and traders.
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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 Berk Brand of Bendroflumethiazide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Berk Brand of Bendroflumethiazide 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 Berk Brand of Bendroflumethiazide 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 Berk Brand of Bendroflumethiazide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Berk Brand of Bendroflumethiazide NDC to their finished compounded human drug products, they may choose to do so.
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