Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

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01 9Active
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01 1218MF10971
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01 120130507-176-I-164-01
02 120130507-176-I-164-01(1)
03 120241230-176-I-684-02
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01 10406-1492
02 10406-1493
03 112707-037
04 138779-0767
05 149452-4836
06 149812-0195
07 150396-0200
08 150396-0202
09 150396-0203
10 151634-2018
11 151927-0327
12 152465-101
13 152465-102
14 152465-107
15 160870-0288
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17 162756-629
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Certificate Number : CEP 2022-086 - Rev 00
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 729
Status : Valid
Date of Issue : 2025-02-11
Valid Till : 2027-06-09
Written Confirmation Number : WC-0278
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-15
Pay. Date : 2013-01-23
DMF Number : 23142
Submission : 2009-09-30
Status : Active
Type : II
Certificate Number : CEP 1996-050 - Rev 08
Issue Date : 2025-10-20
Type : Chemical
Substance Number : 729
Status : Valid
Registration Number : 218MF10971
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2006-12-01
Latest Date of Registration :
Registrant Name : Mundipharma Korea Co., Ltd.
Registration Date : 2013-06-14
Registration Number : 20130507-176-I-164-01(1)
Manufacturer Name : Sanofi Winthrop Industrie
Manufacturer Address : Route d'Avignon 30390 Aramon France
| Available Reg Filing : CN |
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-0203
Start Marketing Date : 2020-07-20
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-23
Pay. Date : 2012-11-26
DMF Number : 20745
Submission : 2007-07-31
Status : Active
Type : II
Certificate Number : R1-CEP 2006-261 - Rev 04
Issue Date : 2020-02-21
Type : Chemical
Substance Number : 729
Status : Valid
NDC Package Code : 12707-037
Start Marketing Date : 2017-12-11
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
NDC Package Code : 60870-0288
Start Marketing Date : 1986-10-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Deccan Nutraceuticals: A global leader in the integrated development, manufacturing, and marketing of pharmaceutical products.
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-14
Pay. Date : 2012-12-07
DMF Number : 24633
Submission : 2011-02-15
Status : Active
Type : II
Certificate Number : R1-CEP 2014-125 - Rev 01
Issue Date : 2021-02-24
Type : Chemical
Substance Number : 729
Status : Valid
NDC Package Code : 51634-2018
Start Marketing Date : 2025-06-01
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Siegfried – A global CDMO delivering integrated pharmaceutical development and manufacturing solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-08-08
Pay. Date : 2013-01-28
DMF Number : 24668
Submission : 2011-02-24
Status : Active
Type : II
Certificate Number : CEP 2011-126 - Rev 03
Issue Date : 2026-02-11
Type : Chemical
Substance Number : 729
Status : Valid
NDC Package Code : 65724-0053
Start Marketing Date : 2019-05-31
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Naloxone Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Naloxone Hydrochloride manufacturer or Naloxone Hydrochloride supplier for your needs.
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A NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NALOXONE HYDROCHLORIDE AND PENTAZOCINE 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 NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE supplier is an individual or a company that provides NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE active pharmaceutical ingredient (API) or NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE finished formulations upon request. The NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE suppliers may include NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 28 companies offering NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE
Get in contact with the supplier of your choice: