01 1Cadila Pharmaceuticals Limited
02 1Fagron Inc
03 1Glenmark Life Sciences Limited
04 1Hetero Labs Limited
05 3MYLAN LABORATORIES LIMITED
06 1Medisca Inc.
07 2Morepen Laboratories Limited
08 1Professional Compounding Centers of America dba PCCA
09 1Quimica Sintetica S.A.
10 1Rolabo Outsourcing S.L.
11 1Spectrum Laboratory Products, Inc.
12 1Tianish Laboratories Private Limited
13 2Vasudha Pharma Chem Limited
01 7LORATADINE
02 9Loratadine
03 1Loratadine Micronized
01 8India
02 1Netherlands
03 2Spain
04 5U.S.A
05 1United Kingdom
NDC Package Code : 51552-1210
Start Marketing Date : 2011-10-31
End Marketing Date : 2027-04-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-2857
Start Marketing Date : 2015-04-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62993-0801
Start Marketing Date : 1996-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62993-0803
Start Marketing Date : 2000-11-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-4219
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53069-0700
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63827-0001
Start Marketing Date : 2011-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4135
Start Marketing Date : 2009-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-684
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-802
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Loratadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loratadine, including repackagers and relabelers. The FDA regulates Loratadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loratadine 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 Loratadine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loratadine supplier is an individual or a company that provides Loratadine active pharmaceutical ingredient (API) or Loratadine finished formulations upon request. The Loratadine suppliers may include Loratadine API manufacturers, exporters, distributors and traders.
click here to find a list of Loratadine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Loratadine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Loratadine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Loratadine 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.
The NDC directory also contains data on finished compounded human drug products that contain Loratadine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Loratadine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Loratadine suppliers with NDC on PharmaCompass.
We have 13 companies offering Loratadine
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
