Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Limited
02 1Cheng Fong Chemical Co., Ltd.
03 1Embio Limited
04 1Professional Compounding Centers of America
05 1Professional Compounding Centers of America dba PCCA
06 5Siegfried PharmaChemikalien Minden GmbH
07 1Spectrum Laboratory Products, Inc.
08 1Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
01 2PSEUDOEPHEDRINE HYDROCHLORIDE
02 9Pseudoephedrine Hydrochloride
03 1Pseudoephedrine hydrochloride
01 2China
02 2India
03 5Switzerland
04 1U.S.A
05 2United Kingdom
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-801
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58747-7538
Start Marketing Date : 1992-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60646-102
Start Marketing Date : 1998-12-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0125
Start Marketing Date : 2021-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1159
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65724-4400
Start Marketing Date : 2010-03-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4401
Start Marketing Date : 2002-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4407
Start Marketing Date : 2011-06-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65724-4415
Start Marketing Date : 2002-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6110
Start Marketing Date : 1992-10-01
End Marketing Date : 2025-08-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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A Sine-Off Maximum Strength No Drowsiness Formula Caplets manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sine-Off Maximum Strength No Drowsiness Formula Caplets, including repackagers and relabelers. The FDA regulates Sine-Off Maximum Strength No Drowsiness Formula Caplets manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sine-Off Maximum Strength No Drowsiness Formula Caplets 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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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Sine-Off Maximum Strength No Drowsiness Formula Caplets as an active pharmaceutical ingredient (API).
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Pharmaceutical companies that manufacture Sine-Off Maximum Strength No Drowsiness Formula Caplets as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
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We have 7 companies offering Sine-Off Maximum Strength No Drowsiness Formula Caplets
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