octreotide acetate
Generic: octreotide acetate
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
octreotide acetate
Generic Name
octreotide acetate
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
octreotide acetate 1000 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
23155-686
Product ID
23155-686_b90ce9b0-5886-4b4f-a721-9698fa28a7ec
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203765
Listing Expiration
2026-12-31
Marketing Start
2022-05-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155686
Hyphenated Format
23155-686
Supplemental Identifiers
RxCUI
UPC
UNII
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
octreotide acetate (source: ndc)
Generic Name
octreotide acetate (source: ndc)
Application Number
ANDA203765 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1000 ug/mL
Packaging
- 5 mL in 1 VIAL, GLASS (23155-686-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "b90ce9b0-5886-4b4f-a721-9698fa28a7ec", "openfda": {"upc": ["0323155689310", "0323155687316", "0323155688313"], "unii": ["75R0U2568I"], "rxcui": ["312068", "312069", "312070", "312071", "314152"], "spl_set_id": ["ffaf9462-cdd8-433b-8b03-464a35577fe9"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, GLASS (23155-686-31)", "package_ndc": "23155-686-31", "marketing_start_date": "20220525"}], "brand_name": "OCTREOTIDE ACETATE", "product_id": "23155-686_b90ce9b0-5886-4b4f-a721-9698fa28a7ec", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Somatostatin Analog [EPC]", "Somatostatin Receptor Agonists [MoA]"], "product_ndc": "23155-686", "generic_name": "octreotide acetate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OCTREOTIDE ACETATE", "active_ingredients": [{"name": "OCTREOTIDE ACETATE", "strength": "1000 ug/mL"}], "application_number": "ANDA203765", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}