Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
01 1Pharm-RX Chemical
02 1Jai Radhe Sales
03 35N Plus Lubeck GmbH
04 1FIRST RARE MATERIALS CO LTD
05 1JQC (Huayin) Pharmaceutical Co.,Ltd
06 1Laboratorios Imperiales, S.A. de C.V.
07 1OMICRON QUIMICA SA
08 1Siegfried AG
01 3Canada
02 2China
03 1France
04 1India
05 1Mexico
06 1Switzerland
07 1U.S.A
01 5Active
02 2Inactive
03 3Blank
01 10Blank
01 10Blank
01 10Blank
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
Jai Radhe Sales is your partner for all your sourcing needs.
GDUFA
DMF Review : N/A
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DMF Number : 25360
Submission : 2011-10-04
Status : Active
Type : II
NDC Package Code : 57465-200
Start Marketing Date : 1986-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
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DMF Number : 27871
Submission : 2013-12-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9660
Submission : 1992-04-20
Status : Active
Type : II
NDC Package Code : 47167-4444
Start Marketing Date : 1992-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16327
Submission : 2002-12-23
Status : Active
Type : II
NDC Package Code : 47167-4444
Start Marketing Date : 1992-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36384
Submission : 2021-12-15
Status : Active
Type : II
NDC Package Code : 47167-4444
Start Marketing Date : 1992-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11889
Submission : 1996-03-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
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DMF Number : 572
Submission : 1963-05-29
Status : Inactive
Type : II
A Pepto-bismol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pepto-bismol, including repackagers and relabelers. The FDA regulates Pepto-bismol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pepto-bismol 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 Pepto-bismol supplier is an individual or a company that provides Pepto-bismol active pharmaceutical ingredient (API) or Pepto-bismol finished formulations upon request. The Pepto-bismol suppliers may include Pepto-bismol API manufacturers, exporters, distributors and traders.
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