octreoscan

Generic: indium in -111 pentetreotide

Labeler: curium us llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name octreoscan
Generic Name indium in -111 pentetreotide
Labeler curium us llc
Dosage Form KIT
Manufacturer
Curium US LLC

Identifiers & Regulatory

Product NDC 69945-050
Product ID 69945-050_3d7648ab-7b11-495d-925c-3a991065237e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020314
Listing Expiration 2026-12-31
Marketing Start 2015-10-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69945050
Hyphenated Format 69945-050

Packaging Origin

Original Packager
true

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 octreoscan (source: ndc)
Generic Name indium in -111 pentetreotide (source: ndc)
Application Number NDA020314 (source: ndc)

Resolved Composition

Strengths
  • 10 mcg
  • 2 mg
  • 4.9 mg
  • 0.37 mg
  • 10 mg
  • 1.1 ml
  • 3.5 mcg/ml
  • 1.2 mcg/ml
  • 25 g
source: label
Packaging
  • 1 KIT in 1 BOX (69945-050-40) * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "3d7648ab-7b11-495d-925c-3a991065237e", "openfda": {"spl_set_id": ["93d8f3b2-1216-41dc-a63d-0e812b33891d"], "manufacturer_name": ["Curium US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 BOX (69945-050-40)  *  1 mL in 1 VIAL, GLASS *  1 mL in 1 VIAL, GLASS", "package_ndc": "69945-050-40", "marketing_start_date": "20151014"}], "brand_name": "OCTREOSCAN", "product_id": "69945-050_3d7648ab-7b11-495d-925c-3a991065237e", "dosage_form": "KIT", "product_ndc": "69945-050", "generic_name": "Indium In -111 Pentetreotide", "labeler_name": "Curium US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OCTREOSCAN", "application_number": "NDA020314", "marketing_category": "NDA", "marketing_start_date": "20151014", "listing_expiration_date": "20261231"}