triptodur

Generic: triptorelin

Labeler: azurity pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name triptodur
Generic Name triptorelin
Labeler azurity pharmaceuticals, inc.
Dosage Form KIT
Manufacturer
Azurity Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 24338-150
Product ID 24338-150_1c06d8b5-edbc-4de7-a423-7588069d3c38
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA208956
Listing Expiration 2026-12-31
Marketing Start 2017-09-08

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24338150
Hyphenated Format 24338-150

Supplemental Identifiers

RxCUI
905053 1944389

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 triptodur (source: ndc)
Generic Name triptorelin (source: ndc)
Application Number NDA208956 (source: ndc)

Resolved Composition

Strengths
  • 22.5 mg
  • 2 ml
source: label
Packaging
  • 1 KIT in 1 CARTON (24338-150-20) * 2 mL in 1 VIAL * 2 mL in 1 SYRINGE, 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": "1c06d8b5-edbc-4de7-a423-7588069d3c38", "openfda": {"rxcui": ["905053", "1944389"], "spl_set_id": ["f41380e7-b830-432d-a5f5-a872932f107e"], "manufacturer_name": ["Azurity Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (24338-150-20)  *  2 mL in 1 VIAL *  2 mL in 1 SYRINGE, GLASS", "package_ndc": "24338-150-20", "marketing_start_date": "20170908"}], "brand_name": "TRIPTODUR", "product_id": "24338-150_1c06d8b5-edbc-4de7-a423-7588069d3c38", "dosage_form": "KIT", "product_ndc": "24338-150", "generic_name": "triptorelin", "labeler_name": "Azurity Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRIPTODUR", "application_number": "NDA208956", "marketing_category": "NDA", "marketing_start_date": "20170908", "listing_expiration_date": "20261231"}