netspot
Generic: 68ga-dotatate
Labeler: advanced accelerator applications usa, incDrug Facts
Product Profile
Brand Name
netspot
Generic Name
68ga-dotatate
Labeler
advanced accelerator applications usa, inc
Dosage Form
KIT
Routes
Manufacturer
Identifiers & Regulatory
Product NDC
69488-001
Product ID
69488-001_3a8e7db3-9df3-4957-809d-e194516874c0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208547
Listing Expiration
2027-12-31
Marketing Start
2016-06-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69488001
Hyphenated Format
69488-001
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
netspot (source: ndc)
Generic Name
68ga-dotatate (source: ndc)
Application Number
NDA208547 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mcg
- 5 mcg
- 6 mcg
- 20 mg
- 10 ml
- 60 mg
- 56.5 mg
- 1 ml
Packaging
- 1 KIT in 1 KIT (69488-001-40) * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (0)
No ingredient records.
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3a8e7db3-9df3-4957-809d-e194516874c0", "openfda": {"spl_set_id": ["b2b3be70-17d8-4093-896c-f1c54a2cf242"], "manufacturer_name": ["Advanced Accelerator Applications USA, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (69488-001-40) * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "69488-001-40", "marketing_start_date": "20160601"}], "brand_name": "NETSPOT", "product_id": "69488-001_3a8e7db3-9df3-4957-809d-e194516874c0", "dosage_form": "KIT", "product_ndc": "69488-001", "generic_name": "68Ga-DOTATATE", "labeler_name": "Advanced Accelerator Applications USA, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NETSPOT", "application_number": "NDA208547", "marketing_category": "NDA", "marketing_start_date": "20160601", "listing_expiration_date": "20271231"}