Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1KALINTIS HEALTHCARE PRIVATE LIMITED
03 1MYLAN LABORATORIES LIMITED
04 1Pisgah Laboratories Inc
05 1SpecGx LLC
01 1DIPHENOXYLATE HYDROCHLORIDE
02 1DIPHENOXYLATE HYDROCHLORIDE WITH ATROPINE SULFATE
03 1Diphenoxylate HCl
04 2Diphenoxylate Hydrochloride
01 1India
02 1Ireland
03 3U.S.A
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 49812-0248
Start Marketing Date : 2014-01-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72166-011
Start Marketing Date : 2021-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0406-1592
Start Marketing Date : 2013-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63804-0018
Start Marketing Date : 2023-08-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-881
Start Marketing Date : 2017-02-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Diphenoxylate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diphenoxylate Hydrochloride, including repackagers and relabelers. The FDA regulates Diphenoxylate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diphenoxylate 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 Diphenoxylate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diphenoxylate Hydrochloride supplier is an individual or a company that provides Diphenoxylate Hydrochloride active pharmaceutical ingredient (API) or Diphenoxylate Hydrochloride finished formulations upon request. The Diphenoxylate Hydrochloride suppliers may include Diphenoxylate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Diphenoxylate 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 Diphenoxylate Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Diphenoxylate 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 Diphenoxylate 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 Diphenoxylate Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Diphenoxylate Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Diphenoxylate Hydrochloride suppliers with NDC on PharmaCompass.
We have 5 companies offering Diphenoxylate Hydrochloride
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