01 5Ajinomoto Health & Nutrition North America Inc.
01 1AMINO ACID MIXTURE 219 (MIX C)
02 1AMINO ACID MIXTURE BLEND D
03 1AMINO ACID MIXTURE BLEND F
04 1AMINO ACID MIXTURE BLEND PMCB - PEDIATRIC BLEND
05 1AMINO ACID MIXTURE CS-TB
01 5Japan
ALANINE; ARGININE; GLYCINE; HISTIDINE; ISOLEUCINE; LEUCINE; LYSINE HYDROCHLORIDE; METHIONINE; PHENYLALANINE; PROLINE; SERINE; THREONINE; TRYPTOPHAN; TYROSINE; VALINE
NDC Package Code : 51495-201
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20.41kg/100kg 11.34kg/100kg 10.15kg/100kg 4.73kg/100kg 5.91kg/100kg 7.2kg/100kg 7.15kg/100kg 3.94kg/100kg 5.52kg/100kg 6.7kg/100kg 4.93kg/100kg 4.14kg/100kg 1.77kg/100kg .39kg/100kg 5.72kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
ALANINE; ARGININE; GLYCINE; HISTIDINE; ISOLEUCINE; LEUCINE; LYSINE HYDROCHLORIDE; METHIONINE; PROLINE; SERINE; THREONINE; TYROSINE; VALINE
NDC Package Code : 51495-178
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (22.01kg/100kg 12.23kg/100kg 10.95kg/100kg 5.1kg/100kg 6.38kg/100kg 7.76kg/100kg 7.71kg/100kg 4.25kg/100kg 7.23kg/100kg 5.32kg/100kg 4.47kg/100kg .43kg/100kg 6.17kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
ALANINE; ARGININE; GLYCINE; HISTIDINE; ISOLEUCINE; LEUCINE; LYSINE HYDROCHLORIDE; METHIONINE; PHENYLALANINE; PROLINE; SERINE; THREONINE; TRYPTOPHAN; TYROSINE; VALINE
NDC Package Code : 51495-203
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (8.5kg/100kg 9.55kg/100kg 4.56kg/100kg 6.4kg/100kg 7.6kg/100kg 9.1kg/100kg 8.5kg/100kg 7.6kg/100kg 5.1kg/100kg 5.3kg/100kg 4.56kg/100kg 5.75kg/100kg 2.42kg/100kg 2.69kg/100kg 12.45kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
ALANINE; ARGININE; ASPARTIC ACID; GLUTAMIC ACID; GLYCINE; HISTIDINE; ISOLEUCINE; LEUCINE; LYSINE ACETATE; METHIONINE; PHENYLALANINE; PROLINE; SERINE; THREONINE; TRYPTOPHAN; TYROSINE; VALINE
NDC Package Code : 51495-199
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (14.01kg/100kg 9.49kg/100kg 2.8kg/100kg 4.84kg/100kg 6.72kg/100kg 5.77kg/100kg 4.84kg/100kg 6.72kg/100kg 10.75kg/100kg 4.84kg/100kg 6.72kg/100kg 5.77kg/100kg 3.82kg/100kg 4.84kg/100kg 1.61kg/100kg .252kg/100kg 6.2kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
ALANINE; ARGININE; ASPARTIC ACID; CYSTEINE; GLUTAMIC ACID; GLYCINE; HISTIDINE; ISOLEUCINE; LEUCINE; LYSINE HYDROCHLORIDE; METHIONINE; ORNITHINE HYDROCHLORIDE; PHENYLALANINE; PROLINE; SERINE; TAURINE; THREONINE; TRYPTOPHAN; TYROSINE; VALINE
NDC Package Code : 51495-205
Start Marketing Date : 2022-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (7.8kg/100kg 8.2kg/100kg 5.85kg/100kg 1.85kg/100kg 9.75kg/100kg 3.92kg/100kg 3.72kg/100kg 6.5kg/100kg 9.75kg/100kg 12.05kg/100kg 2.35kg/100kg 3.1kg/100kg 4.12kg/100kg 2.94kg/100kg 3.92kg/100kg .59kg/100kg 3.62kg/100kg 1.97kg/100kg .76kg/100kg 7.4kg/100kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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A FREAMINE III 8.5% manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FREAMINE III 8.5%, including repackagers and relabelers. The FDA regulates FREAMINE III 8.5% manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FREAMINE III 8.5% 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 FREAMINE III 8.5% supplier is an individual or a company that provides FREAMINE III 8.5% active pharmaceutical ingredient (API) or FREAMINE III 8.5% finished formulations upon request. The FREAMINE III 8.5% suppliers may include FREAMINE III 8.5% API manufacturers, exporters, distributors and traders.
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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 FREAMINE III 8.5% as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for FREAMINE III 8.5% 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 FREAMINE III 8.5% 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 FREAMINE III 8.5% and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a FREAMINE III 8.5% NDC to their finished compounded human drug products, they may choose to do so.
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