01 Alembic Pharmaceuticals Limited (1)
02 Boehringer Ingelheim GmbH (2)
03 CSPC New Nova Pharmaceutical (1)
04 Concordia Labs Inc (3)
05 F. Hoffmann-La Roche (8)
06 Hainan Poly Pharm (1)
07 Hangzhou Minsheng Binjiang Pharmaceutical CO., Ltd (1)
08 Mallinckrodt Pharmaceuticals (3)
09 Roche Diagnostics GmbH (1)
10 Shandong Xinhua Pharmaceutical (1)
11 Siegfried AG (2)
12 The Dow Chemical Company (1)
13 Blank (12)
01 7 BETA-HYDROXYPROPYL THEOPHYLLINE (1)
02 8 - BROMOTHEOPHYLLINE (1)
03 ACCURBRON, S.R. (CONTROLLED RELEASE THEOPHYLLINE) (1)
04 AEROLATE CONTROLLED-RELEASE CAPSULES CONTAINING THEOPHYLLINE (1)
05 DIHYDROXYPROPYL-THEOPHYLLIN (1)
06 DIHYDROXYPROPYLTHEOPHYLLINE (DYPHYLLINE) (1)
07 ELIXOPHYLLIN SUSTAINED RELEASE CAPSULES 125MG (THEOPHYLLINE) (1)
08 ELIXOPHYLLIN SUSTAINED RELEASE CAPSULES 250MG. (THEOPHYLLINE) (1)
09 PAMABROM (8-BROMOTHEOPHYLLINE-ISOBUTANOLAMINE) (1)
10 SOMOPHYLLIN CONTROLLED RELEASE THEOPHYLLINE 250MG (1)
11 THEOPHILLINE S.R. CAPSULES 250MG (1)
12 THEOPHYL S.R. CAPS 125MG & 250MG (THEOPHYLLINE)-FOR KNOLL PHARMA CO. (1)
13 THEOPHYLLIN (1)
14 THEOPHYLLINE (4)
15 THEOPHYLLINE (ANHYDROUS) (1)
16 THEOPHYLLINE (ANHYDROUS) USP (1)
17 THEOPHYLLINE ANHYDROUS (1)
18 THEOPHYLLINE CAP (1)
19 THEOPHYLLINE CAPS., 250MG (1)
20 THEOPHYLLINE CAPSULES, T.D. (1)
21 THEOPHYLLINE CONTROLLED RELEASE BEADS (2)
22 THEOPHYLLINE EXTENDED RELEASE CAPSULES (1)
23 THEOPHYLLINE HYDROUS (1)
24 THEOPHYLLINE MONOHYDRATE (1)
25 THEOPHYLLINE PHARMAZOME TM POWDER (1)
26 THEOPHYLLINE R 85 D/02 (1)
27 THEOPHYLLINE S.R. CAPS 300MG (1)
28 THEOPHYLLINE S.R. CAPSULES 125MG (1)
29 THEOPHYLLINE S.R. CAPSULES, 250 MG. (1)
30 THEOPHYLLINE SR62.5MG MNFG IN ST.LOUIS,MO FOR SCHERING,KENILWORTH N.J. (1)
31 THEOPHYLLINE SUSTAINED RELEASE CAPSULES (BY-158) (1)
32 THEOPHYLLINE SUSTAINED RELEASE CAPSULES, 125 MG. (1)
33 THEOPHYLLINE, ANHYDROUS (1)
01 Canada (3)
02 China (4)
03 Germany (3)
04 India (1)
05 Ireland (3)
06 Switzerland (10)
07 U.S.A (1)
08 Blank (12)
01 Active (4)
02 Inactive (33)
01 Complete (1)
02 Blank (36)
92
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A MolPort-001-737-342 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-737-342, including repackagers and relabelers. The FDA regulates MolPort-001-737-342 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-737-342 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 MolPort-001-737-342 supplier is an individual or a company that provides MolPort-001-737-342 active pharmaceutical ingredient (API) or MolPort-001-737-342 finished formulations upon request. The MolPort-001-737-342 suppliers may include MolPort-001-737-342 API manufacturers, exporters, distributors and traders.
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A MolPort-001-737-342 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-737-342 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-737-342 DMFs exist exist since differing nations have different regulations, such as MolPort-001-737-342 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-737-342 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-737-342 USDMF includes data on MolPort-001-737-342's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-737-342 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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