Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Limited
02 1Swati Spentose Private Limited
03 1Adare Pharmaceuticals Inc
04 2Anqiu Lu'an Pharmaceutical Co., Ltd.
05 1Asclemed USA Inc.
06 1Kalchem International inc
07 1Kongo Chemical Co., Ltd.
08 1L. Perrigo Company
09 1LETCO MEDICAL, LLC
10 1Medisca Inc.
11 1Professional Compounding Centers of America dba PCCA
12 1QIDONG DONGYUE PHARMACEUTICAL CO., LTD.
13 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
14 1SAMANTA ORGANICS PRIVATE LIMITED
15 1Spectrum Laboratory Products, Inc.
16 2Wanbury Limited
01 2Acetaminophen/Diphenhydramine HCL
02 1DIPHENHYDRAMINE
03 1DIPHENHYDRAMINE HCL
04 3DIPHENHYDRAMINE HYDROCHLORIDE
05 1Diphenhydramine Hcl
06 8Diphenhydramine Hydrochloride
07 1Diphenhydramine hydrochloride
08 1acetaminophen, diphenhydramine hydrochloride, phenylephrine hydrochloride
01 1China
02 5India
03 1Ireland
04 1Italy
05 1Japan
06 6U.S.A
07 1United Kingdom
08 2Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-6000
Start Marketing Date : 2013-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SWATI – Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
NDC Package Code : 52119-013
Start Marketing Date : 2016-05-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12294-9997
Start Marketing Date : 1978-01-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0282
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1079
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
NDC Package Code : 0113-9445
Start Marketing Date : 2014-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER, FOR SOLUTION (650mg/1 25mg/1 10mg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 12711-4367
Start Marketing Date : 1980-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 49452-2640
Start Marketing Date : 1990-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
NDC Package Code : 59644-9926
Start Marketing Date : 2016-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (.5kg/.5kg .5kg/.5kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
NDC Package Code : 59644-9927
Start Marketing Date : 2016-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg 1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Diphenhydramine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Diphenhydramine Hydrochloride API Price utilized in the formulation of products. Diphenhydramine Hydrochloride API Price is not always fixed or binding as the Diphenhydramine Hydrochloride Price is obtained through a variety of data sources. The Diphenhydramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ziradryl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ziradryl, including repackagers and relabelers. The FDA regulates Ziradryl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ziradryl 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 Ziradryl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ziradryl supplier is an individual or a company that provides Ziradryl active pharmaceutical ingredient (API) or Ziradryl finished formulations upon request. The Ziradryl suppliers may include Ziradryl API manufacturers, exporters, distributors and traders.
click here to find a list of Ziradryl 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 Ziradryl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ziradryl 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 Ziradryl 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 Ziradryl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ziradryl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ziradryl suppliers with NDC on PharmaCompass.
We have 15 companies offering Ziradryl
Get in contact with the supplier of your choice:
