01 1Apotex Pharmachem
02 1Boehringer Ingelheim GmbH
03 1ChemSource
04 1Corden Pharma Bergamo S.p.A
05 3Fako Ilaçlari A.S. TR 34390 Istanbul
06 1Genpharma
07 1Heumann
08 1Maprimed
09 1NOVOPHARM LTD
10 1Orchev Pharma
11 2Quimica Sintetica
12 2RANBAXY LABORATORIES LIMITED
13 4SMS Pharmaceuticals
14 2Saraca Laboratories Limited
15 1Shasun Chemicals and Drugs Ltd
16 2Solara Active Pharma Sciences
17 2UQUIFA
18 2Wockhardt
19 3Blank
01 1RANITIDINE HCI (FORM-I)
02 1RANITIDINE HCI FORM 1 DRUG SUBSTANCE
03 1RANITIDINE HCL
04 1RANITIDINE HCL FORM 1
05 1RANITIDINE HCL USP
06 10RANITIDINE HYDROCHLORIDE
07 1RANITIDINE HYDROCHLORIDE (CRYSTALLINE FORM 1)
08 1RANITIDINE HYDROCHLORIDE (FORM-II)
09 2RANITIDINE HYDROCHLORIDE FORM I BULK
10 1RANITIDINE HYDROCHLORIDE FORM II
11 5RANITIDINE HYDROCHLORIDE USP
12 1RANITIDINE HYDROCHLORIDE USP (FORM II)
13 1RANITIDINE HYDROCHLORIDE USP (PROCESS -2)
14 1RANITIDINE HYDROCHLORIDE USP (UNIT-VII)
15 1RANITIDINE HYDROCHLORIDE USP FORM 1
16 1RANITIDINE HYDROCHLORIDE USP, FORM 1
17 1RANITIDINE HYDROCHLORIDE, USP (FORM II)
18 1RANITIDINE HYDROCHLORIDE-FORM 1
01 1Argentina
02 2Canada
03 2Germany
04 14India
05 1Italy
06 1Morocco
07 4Spain
08 3Turkey
09 1U.S.A
10 3Blank
01 3Active
02 29Inactive
01 2Complete
02 30Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10989
Submission : 1994-07-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10885
Submission : 1994-04-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25851
Submission : 2012-02-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8494
Submission : 1990-03-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10516
Submission : 1993-10-05
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-07-11
Pay. Date : 2017-05-31
DMF Number : 31575
Submission : 2017-03-16
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-15
Pay. Date : 2013-12-09
DMF Number : 8288
Submission : 1989-11-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10273
Submission : 1993-05-27
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8953
Submission : 1991-01-29
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7528
Submission : 1988-06-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Ranitidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ranitidine Hydrochloride, including repackagers and relabelers. The FDA regulates Ranitidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ranitidine 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 Ranitidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ranitidine Hydrochloride supplier is an individual or a company that provides Ranitidine Hydrochloride active pharmaceutical ingredient (API) or Ranitidine Hydrochloride finished formulations upon request. The Ranitidine Hydrochloride suppliers may include Ranitidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ranitidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ranitidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Ranitidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Ranitidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Ranitidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ranitidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Ranitidine Hydrochloride USDMF includes data on Ranitidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ranitidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ranitidine Hydrochloride suppliers with USDMF on PharmaCompass.
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