octreotide acetate

Generic: octreotide acetate

Labeler: teva pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name octreotide acetate
Generic Name octreotide acetate
Labeler teva pharmaceuticals, inc.
Dosage Form KIT
Routes
INTRAMUSCULAR
Manufacturer
Teva Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0480-9259
Product ID 0480-9259_2e77a034-b0ae-4694-8ac0-ae1319754d3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210317
Listing Expiration 2026-12-31
Marketing Start 2024-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04809259
Hyphenated Format 0480-9259

Supplemental Identifiers

RxCUI
898589 898601 898605

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 octreotide acetate (source: ndc)
Generic Name octreotide acetate (source: ndc)
Application Number ANDA210317 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 10 mg
  • 20 mg
  • 30 mg
  • 2 ml
  • 10 mg/8 ml
  • 20 mg/8 ml
  • 30 mg/8 ml
source: label
Packaging
  • 1 KIT in 1 KIT (0480-9259-08) * 8 mL in 1 VIAL, SINGLE-DOSE (0480-9258-01) * 2 mL in 1 SYRINGE (0480-9263-21)
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "2e77a034-b0ae-4694-8ac0-ae1319754d3a", "openfda": {"rxcui": ["898589", "898601", "898605"], "spl_set_id": ["d9739ea6-74de-4a41-a806-6e827a23cedb"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (0480-9259-08)  *  8 mL in 1 VIAL, SINGLE-DOSE (0480-9258-01)  *  2 mL in 1 SYRINGE (0480-9263-21)", "package_ndc": "0480-9259-08", "marketing_start_date": "20241001"}], "brand_name": "Octreotide Acetate", "product_id": "0480-9259_2e77a034-b0ae-4694-8ac0-ae1319754d3a", "dosage_form": "KIT", "product_ndc": "0480-9259", "generic_name": "Octreotide Acetate", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Octreotide Acetate", "application_number": "ANDA210317", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}