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Last Updated: December 15, 2025

List of Excipients in API octreotide acetate

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Excipients in NDA-approved (novel) drugs containing octreotide acetate

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Company	Tradename	Ingredient	NDC	Excipient	Potential Generic Entry
Novartis Pharmaceuticals Corporation	SANDOSTATIN	octreotide acetate	0078-0180	LACTIC ACID
Novartis Pharmaceuticals Corporation	SANDOSTATIN	octreotide acetate	0078-0180	MANNITOL
Novartis Pharmaceuticals Corporation	SANDOSTATIN	octreotide acetate	0078-0180	SODIUM BICARBONATE
Novartis Pharmaceuticals Corporation	SANDOSTATIN	octreotide acetate	0078-0180	WATER
>Company	>Tradename	>Ingredient	>NDC	>Excipient	>Potential Generic Entry

Excipients in ANDA-approved (generic) drugs containing octreotide acetate

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Company	Ingredient	NDC	Excipient
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174	LACTIC ACID, L-
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174	SODIUM CHLORIDE
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174	SODIUM HYDROXIDE
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174	WATER
>Company	>Ingredient	>NDC	>Excipient

Detailed excipient profiles for octreotide acetate

Excipient focus: ACETIC ACID

octreotide acetate drug variants containing ACETIC ACID

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Company	Ingredient	NDC
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
Sagent Pharmaceuticals	octreotide acetate	25021-463
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing ACETIC ACID

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
>Company	>Ingredient	>NDC

Excipient focus: LACTIC ACID

octreotide acetate drug variants containing LACTIC ACID

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
Gland Pharma Limited	octreotide acetate	68083-515
Gland Pharma Limited	octreotide acetate	68083-517
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing LACTIC ACID

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
>Company	>Ingredient	>NDC

Excipient focus: LACTIC ACID, L-

octreotide acetate drug variants containing LACTIC ACID, L-

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Mylan Institutional LLC	octreotide acetate	67457-239
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing LACTIC ACID, L-

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
>Company	>Ingredient	>NDC

Excipient focus: MANNITOL

octreotide acetate drug variants containing MANNITOL

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing MANNITOL

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
Sagent Pharmaceuticals	octreotide acetate	25021-463
>Company	>Ingredient	>NDC

Excipient focus: PHENOL

octreotide acetate drug variants containing PHENOL

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Company	Ingredient	NDC
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
Gland Pharma Limited	octreotide acetate	68083-515
USV North America Inc	octreotide acetate	76135-005
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing PHENOL

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Sagent Pharmaceuticals	octreotide acetate	25021-451
>Company	>Ingredient	>NDC

Excipient focus: SODIUM ACETATE

octreotide acetate drug variants containing SODIUM ACETATE

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Company	Ingredient	NDC
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
Sagent Pharmaceuticals	octreotide acetate	25021-463
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing SODIUM ACETATE

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
>Company	>Ingredient	>NDC

Excipient focus: SODIUM BICARBONATE

octreotide acetate drug variants containing SODIUM BICARBONATE

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
Gland Pharma Limited	octreotide acetate	68083-515
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing SODIUM BICARBONATE

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
>Company	>Ingredient	>NDC

Excipient focus: SODIUM CHLORIDE

octreotide acetate drug variants containing SODIUM CHLORIDE

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
Sagent Pharmaceuticals	octreotide acetate	25021-463
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing SODIUM CHLORIDE

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Hainan Shuangcheng Pharmaceuticals Co Ltd	octreotide acetate	52958-046
Sun Pharmaceutical Industries Inc	octreotide acetate	62756-452
>Company	>Ingredient	>NDC

Excipient focus: SODIUM HYDROXIDE

octreotide acetate drug variants containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Mylan Institutional LLC	octreotide acetate	67457-239
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing SODIUM HYDROXIDE

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
Sagent Pharmaceuticals	octreotide acetate	25021-451
>Company	>Ingredient	>NDC

Excipient focus: WATER

octreotide acetate drug variants containing WATER

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Company	Ingredient	NDC
Novartis Pharmaceuticals Corporation	octreotide acetate	0078-0180
Hikma Pharmaceuticals USA Inc	octreotide acetate	0641-6174
Teva Parenteral Medicines Inc	octreotide acetate	0703-3301
Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	octreotide acetate	23155-685
>Company	>Ingredient	>NDC

octreotide acetate drug variants not containing WATER

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Company	Ingredient	NDC
Fresenius Kabi USA LLC	octreotide acetate	63323-365
>Company	>Ingredient	>NDC

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