sandostatin lar depot
Generic: octreotide acetate
Labeler: novartis pharmaceuticals corporationDrug Facts
Product Profile
Brand Name
sandostatin lar depot
Generic Name
octreotide acetate
Labeler
novartis pharmaceuticals corporation
Dosage Form
KIT
Manufacturer
Identifiers & Regulatory
Product NDC
0078-0825
Product ID
0078-0825_2a2ad59f-21cd-4734-9c4b-0154e9db1642
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021008
Listing Expiration
2026-12-31
Marketing Start
2016-07-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00780825
Hyphenated Format
0078-0825
Supplemental Identifiers
RxCUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sandostatin lar depot (source: ndc)
Generic Name
octreotide acetate (source: ndc)
Application Number
NDA021008 (source: ndc)
Resolved Composition
Strengths
- 10 mg
- 20 mg
- 30 mg
- 2 ml
- 10 mg/6 ml
- 20 mg/6 ml
- 30 mg/6 ml
Packaging
- 1 KIT in 1 KIT (0078-0825-81) * 2 mL in 1 SYRINGE * 6 mL in 1 VIAL (0078-0804-61)
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"spl_id": "2a2ad59f-21cd-4734-9c4b-0154e9db1642", "openfda": {"rxcui": ["898589", "898591", "898601", "898603", "898605", "898607"], "spl_set_id": ["d0b7fe9e-7000-4b79-ba3b-291ce92c14f9"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (0078-0825-81) * 2 mL in 1 SYRINGE * 6 mL in 1 VIAL (0078-0804-61)", "package_ndc": "0078-0825-81", "marketing_start_date": "20160722"}], "brand_name": "Sandostatin LAR Depot", "product_id": "0078-0825_2a2ad59f-21cd-4734-9c4b-0154e9db1642", "dosage_form": "KIT", "product_ndc": "0078-0825", "generic_name": "octreotide acetate", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sandostatin LAR Depot", "application_number": "NDA021008", "marketing_category": "NDA", "marketing_start_date": "20160722", "listing_expiration_date": "20261231"}