01 1ALMON HEALTHCARE PRIVATE LIMITED
02 1Amphastar Nanjing Pharmaceuticals, Inc.
03 1Cambrex Profarmaco Milano Srl
04 1Curia New York, Inc
05 1Curia New York, Inc.
06 1DARMERICA, LLC
07 2Derivados Quimicos
08 1Harman Finochem Limited
09 1MYLAN LABORATORIES LIMITED
10 5Professional Compounding Centers of America dba PCCA
11 1Spectrum Laboratory Products Inc
12 1Spectrum Laboratory Products, Inc.
13 1Syn-Tech Chem. & Pharm. Co. LTD.
14 1Viyash Life Sciences Private Limited
15 2Wuhan Wuyao Pharmaceutical Co., Ltd.
01 1DL-Epinephrine HCl
02 4EPINEPHRINE
03 2EPINEPHRINE HCl RACEPINEPHRINE HCl
04 9Epinephrine
05 1Epinephrine Base
06 4Racepinephrine Hydrochloride
01 2China
02 2India
03 2Spain
04 1Taiwan
05 8U.S.A
06 5United Kingdom
07 1Blank
NDC Package Code : 52221-114
Start Marketing Date : 2018-07-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (3kg/3kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0082
Start Marketing Date : 2012-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0074
Start Marketing Date : 2020-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0110
Start Marketing Date : 2020-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0337
Start Marketing Date : 2024-05-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1715
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5014
Start Marketing Date : 2018-05-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-2740
Start Marketing Date : 1989-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6213
Start Marketing Date : 2001-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54871-1095
Start Marketing Date : 2016-06-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Epipen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Epipen, including repackagers and relabelers. The FDA regulates Epipen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Epipen 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 Epipen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Epipen supplier is an individual or a company that provides Epipen active pharmaceutical ingredient (API) or Epipen finished formulations upon request. The Epipen suppliers may include Epipen API manufacturers, exporters, distributors and traders.
click here to find a list of Epipen 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 Epipen as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Epipen 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 Epipen 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 Epipen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Epipen NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Epipen suppliers with NDC on PharmaCompass.
We have 12 companies offering Epipen
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
