01 IOL Chemicals and Pharmaceuticals (1)
02 ACIC Europe API & Pharmaceuticals (1)
03 ACS DOBFAR SPA (1)
04 Adare Pharma Solutions (2)
05 Albemarle Corporation (2)
06 Arch Pharmalabs (1)
07 BASF (2)
08 Catalent Pharma Solutions (4)
09 Cipla (1)
10 F. Hoffmann-La Roche (1)
11 Forest Laboratories, Inc. (1)
12 Granules India Limited (2)
13 Hubei Biocause Heilen Pharmaceutical Co., Ltd (2)
14 IPC Process Center GmbH & Co (1)
15 Industriale Chimica s.r.l. (2)
16 JUHUA GROUP CORP PHARMACEUTICAL FACTORY (1)
17 Luna Chemicals (1)
18 Mallinckrodt Pharmaceuticals (4)
19 NAGASE Europa GmbH (1)
20 Particle Dynamics International, LLC. (1)
21 Pfizer Inc (1)
22 Piramal Enterprises Limited (1)
23 SI Group (2)
24 SMS Pharmaceuticals (1)
25 Shandong Xinhua Pharmaceutical (2)
26 Solara Active Pharma Sciences (4)
27 Wanbury Limited (3)
28 Yonezawa Hamari Chemicals, Ltd. (1)
29 Zambon Switzerland (1)
30 Zibo Xinhua Perrigo Pharmaceutical (1)
31 Blank (13)
01 ADVIL COLD AND SINUS LIQUID GELS (1)
02 ADVIL LIQUI-GELS, 200 MG (1)
03 ADVIL PM LIQUI-GELS (1)
04 ALBE-TAB® IBUPROFEN 90 (1)
05 COMPRESSO IBU 66S (1)
06 COMPRESSO IBU 85 PAR (IBUPROFEN GRANULES DC 85 %) (1)
07 DCI™-63 (IBUPROFEN USP 63%) (1)
08 DEXIBUPROFEN DRUG SUBSTANCE (1)
09 FACILS. AND CONTROL SPECIFS IN KALAMAZOO, MICH. FACILITY (IBUPROFEN) (1)
10 IBUMETIN (IBUPROFEN) TABLETS:200,300,400,&600 MG. (1)
11 IBUPROFEN (14)
12 IBUPROFEN 300MG. LA CAPSULES (1)
13 IBUPROFEN 800 MG C.R. TABLETS (IN SYNCHRON VEHICLE) (1)
14 IBUPROFEN ARGININE (1)
15 IBUPROFEN BP 88/USP XXII (1)
16 IBUPROFEN BULK DRUG (1)
17 IBUPROFEN BULK DRUG SUBSTANCES (1)
18 IBUPROFEN CAPSULES (1)
19 IBUPROFEN DC 85 (1)
20 IBUPROFEN DC GRADE-65% (1)
21 IBUPROFEN DC GRADE-90% (1)
22 IBUPROFEN DC100 (IBUPROFEN PH. EUR., GRANULATED) (1)
23 IBUPROFEN DCI-63 (1)
24 IBUPROFEN DIHYDROCODEINE F.C. TABLETS (1)
25 IBUPROFEN GELATIN/CAP (1)
26 IBUPROFEN S (+) TABLETS (1)
27 IBUPROFEN SODIUM DIHYDRATE (1)
28 IBUPROFEN SOFTGELS, 200 MG. (1)
29 IBUPROFEN TIMED-RELEASE 600 MG. TALBETS (1)
30 IBUPROFEN U.S.P. (1)
31 IBUPROFEN USP (7)
32 IBUPROFEN USP AS PROCESSED IN FACTORIES NO.2, NO. 3, NO.4 CITED IN D (1)
33 IBUPROFEN USP DRUG SUBSTANCE (1)
34 IBUPROFEN USP XX (1)
35 MICROCAPS® IBUPROFEN (1)
36 MICROMASK® IBUPROFEN 72% (1)
37 MOTRIN TAB (1)
38 PROCEDURES FOR THE MANUF OF IBUPROFEN (1)
39 S (+) IBUPROFEN (1)
40 S(+)-IBUPROFEN (1)
41 S-(+)- IBUPROFEN (1)
42 S-(+)-2-(4`-ISOBUTYLPHENYL) PROPIONIC ACID (S-(+)-IBUPROFEN (1)
43 S-IBUPROFEN (1)
01 China (7)
02 Cyprus (1)
03 Germany (4)
04 India (14)
05 Ireland (4)
06 Italy (3)
07 Japan (1)
08 Switzerland (2)
09 U.S.A (13)
10 Blank (13)
01 Active (23)
02 Inactive (39)
01 Complete (10)
02 Blank (52)
27
PharmaCompass offers a list of Ibuprofen 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 Ibuprofen manufacturer or Ibuprofen supplier for your needs.
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PharmaCompass also assists you with knowing the Ibuprofen API Price utilized in the formulation of products. Ibuprofen API Price is not always fixed or binding as the Ibuprofen Price is obtained through a variety of data sources. The Ibuprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AM20060782 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AM20060782, including repackagers and relabelers. The FDA regulates AM20060782 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AM20060782 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 AM20060782 supplier is an individual or a company that provides AM20060782 active pharmaceutical ingredient (API) or AM20060782 finished formulations upon request. The AM20060782 suppliers may include AM20060782 API manufacturers, exporters, distributors and traders.
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A AM20060782 DMF (Drug Master File) is a document detailing the whole manufacturing process of AM20060782 active pharmaceutical ingredient (API) in detail. Different forms of AM20060782 DMFs exist exist since differing nations have different regulations, such as AM20060782 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AM20060782 DMF submitted to regulatory agencies in the US is known as a USDMF. AM20060782 USDMF includes data on AM20060782's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AM20060782 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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