Excluded / Inactive
NDC Directory Crossover & Product Mapping
The following National Drug Codes (NDCs) are directly associated with the clinical concept for Octreotide 100 mcg in 1 mL Injection (RxCUI 312069). This crossover tool provides a verified mapping between standardized RxNorm clinical drug definitions and the specific manufactured products listed in the FDA NDC directory.
Healthcare professionals, pharmacists, and data analysts use this list to identify various brand names, labelers, and commercial packaging variations linked to this semantic clinical drug concept. Each entry below represents a commercial product that fulfills the requirements of this specific clinical identifier.
Manufacturer Quick Index
Found 44 manufactured products
Fresenius Kabi USA, LLC
NDC Product
Human Prescription DrugOctreotide NDC 63323-376
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide NDC 63323-377
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide NDC 63323-378
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide NDC 63323-379
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
GLENMARK PHARMACEUTICALS INC., USA
NDC Product
Human Prescription DrugOctreotide Acetate NDC 68462-896
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 68462-897
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Gland Pharma Limited
NDC Product
Human Prescription DrugOctreotide Acetate NDC 68083-517
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 68083-560
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Hainan Shuangcheng Pharmaceuticals Co., Ltd.
NDC Product
Human Prescription DrugOctreotide Acetate NDC 52958-046
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
NDC Product
Human Prescription DrugOctreotide Acetate NDC 23155-685
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Intravenous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 23155-686
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 23155-687
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 23155-688
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 23155-689
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Hikma Pharmaceuticals USA Inc.
NDC Product
Human Prescription DrugOctreotide Acetate NDC 0641-6174
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 0641-6175
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 0641-6176
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 0641-6177
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 0641-6178
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Meitheal Pharmaceuticals, Inc.
NDC Product
Human Prescription DrugOctreotide Acetate NDC 71288-566
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 71288-567
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 71288-568
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
Novartis Pharmaceuticals Corporation
NDC Product
Human Prescription DrugSandostatin NDC 0078-0180
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandostatin NDC 0078-0181
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- NDA
Active Listing
NDC Product
Human Prescription DrugSandostatin NDC 0078-0182
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- NDA
Active Listing
Sagent Pharmaceuticals
NDC Product
Human Prescription DrugOctreotide Acetate NDC 25021-463
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 25021-464
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 25021-465
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 25021-466
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
NDC Product
Human Prescription DrugOctreotide Acetate NDC 25021-467
- Generic Name
- Octreotide Acetate
- Dosage Form
- Injection, Solution
- Route
- Intravenous; Subcutaneous
- Marketing
- ANDA
Active Listing
USV North America Inc.
NDC Product
Octreotide Acetate NDC 76135-009
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 76135-010
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 76135-011
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Wockhardt Limited
NDC Product
Octreotide Acetate NDC 55648-632
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 55648-633
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 55648-634
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 55648-635
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 55648-636
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
Wockhardt USA LLC.
NDC Product
Octreotide Acetate NDC 64679-632
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 64679-633
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 64679-634
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 64679-635
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
NDC Product
Octreotide Acetate NDC 64679-636
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- ANDA
Excluded / Inactive
