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List of NDC API details of Octreotide Acetate Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Flag Switzerland
Digital Content Digital Content
Octreotide
POWDER (1g/g)
BULK INGREDIENT
52416-109
2018-04-06
2024-12-31
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Octreotide Acetate
POWDER (1g/g)
BULK INGREDIENT FOR ...
52416-123
2020-06-26
2024-12-31
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Octreotide Hydrochloride
POWDER (1g/g)
BULK INGREDIENT
55463-0038
2023-10-23
2024-12-31
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Octreotide
POWDER (1g/g)
EXPORT ONLY
52416-118
2003-08-13
2024-12-31
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Octreotide Acetate
POWDER (1g/g)
BULK INGREDIENT
55463-0035
2019-10-11
2024-12-31
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URL Supplier Web Content
Octreotide
POWDER (1g/g)
BULK INGREDIENT
41524-0007
2012-09-06
2024-12-31
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Flag India
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Octreotide
POWDER (100g/100g)
BULK INGREDIENT
62147-0206
2010-09-01
2024-12-31
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URL Supplier Web Content
Octreotide Acetate
POWDER (100kg/100kg)
BULK INGREDIENT
63415-0065
2020-04-30
2024-12-31
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Octreotide Acetate
POWDER (1kg/kg)
BULK INGREDIENT
59651-004
2015-09-18
2024-12-31
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Flag Spain
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Octreotide
POWDER (1g/g)
BULK INGREDIENT
35207-0002
2013-11-12
2024-12-31
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Octreotide Acetate
POWDER (1g/g)
BULK INGREDIENT
32861-0005
2015-08-18
2024-12-31
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OCTREOTIDE ACETATE
POWDER (1g/g)
BULK INGREDIENT
66558-0192
2021-05-01
2024-12-31
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Octreotide
POWDER (1g/g)
BULK INGREDIENT
73301-004
2020-06-26
2024-12-31
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Octreotide Acetate
POWDER (6g/6g)
BULK INGREDIENT
59149-007
2023-02-20
2024-12-31
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Octreotide Acetate
POWDER (1g/g)
BULK INGREDIENT
65129-1049
2014-03-10
2024-12-31
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octreotide acetate
POWDER (1g/g)
BULK INGREDIENT
76177-119
2019-12-31
2024-12-31
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Octreotide acetate
POWDER (3kg/3kg)
BULK INGREDIENT
50384-6400
2023-07-03
2024-12-31
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OCTREOTIDE ACETATE
POWDER (1kg/kg)
BULK INGREDIENT
65015-840
2015-01-13
2024-12-31
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  • INJECTABLE;INJECTION - EQ 0.05MG BASE/ML
  • INJECTABLE;INJECTION - EQ 0.1MG BASE/ML
  • INJECTABLE;INJECTION - EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
  • INJECTABLE;INJECTION - EQ 0.5MG BASE/ML
  • INJECTABLE;INJECTION - EQ 1MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Looking for 79517-01-4 / Octreotide Acetate API manufacturers, exporters & distributors?

Octreotide Acetate manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Octreotide Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Octreotide Acetate manufacturer or Octreotide Acetate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Octreotide Acetate manufacturer or Octreotide Acetate supplier.

PharmaCompass also assists you with knowing the Octreotide Acetate API Price utilized in the formulation of products. Octreotide Acetate API Price is not always fixed or binding as the Octreotide Acetate Price is obtained through a variety of data sources. The Octreotide Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Octreotide Acetate

Synonyms

Sandostatin, 79517-01-4, Nsc672461, Sandostatin (tn), Acetic acid;10-(4-aminobutyl)-19-[(2-amino-3-phenylpropanoyl)amino]-16-benzyl-n-(1,3-dihydroxybutan-2-yl)-7-(1-hydroxyethyl)-13-(1h-indol-3-ylmethyl)-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carboxamide, Octreotide acetate (usp)

Cas Number

79517-01-4

About Octreotide Acetate

A potent, long-acting synthetic SOMATOSTATIN octapeptide analog that inhibits secretion of GROWTH HORMONE and is used to treat hormone-secreting tumors; DIABETES MELLITUS; HYPOTENSION, ORTHOSTATIC; HYPERINSULINISM; hypergastrinemia; and small bowel fistula.

Octreotide Acetate Manufacturers

A Octreotide Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Octreotide Acetate, including repackagers and relabelers. The FDA regulates Octreotide Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Octreotide Acetate 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 Octreotide Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Octreotide Acetate Suppliers

A Octreotide Acetate supplier is an individual or a company that provides Octreotide Acetate active pharmaceutical ingredient (API) or Octreotide Acetate finished formulations upon request. The Octreotide Acetate suppliers may include Octreotide Acetate API manufacturers, exporters, distributors and traders.

click here to find a list of Octreotide Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Octreotide Acetate NDC

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 Octreotide Acetate as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Octreotide Acetate API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Octreotide Acetate 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Octreotide Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Octreotide Acetate NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Octreotide Acetate suppliers with NDC on PharmaCompass.

Octreotide Acetate Manufacturers | Traders | Suppliers

Octreotide Acetate Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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