supprelin la
Generic: histrelin acetate
Labeler: endo usa, inc.Drug Facts
Product Profile
Brand Name
supprelin la
Generic Name
histrelin acetate
Labeler
endo usa, inc.
Dosage Form
IMPLANT
Routes
Active Ingredients
histrelin acetate 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67979-002
Product ID
67979-002_917e915f-4793-48bf-84c3-50272421616f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA022058
Listing Expiration
2026-12-31
Marketing Start
2007-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67979002
Hyphenated Format
67979-002
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
supprelin la (source: ndc)
Generic Name
histrelin acetate (source: ndc)
Application Number
NDA022058 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 1 VIAL, GLASS in 1 CARTON (67979-002-01) / 1 IMPLANT in 1 VIAL, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "917e915f-4793-48bf-84c3-50272421616f", "openfda": {"upc": ["0367979002016"], "unii": ["QMG7HLD1ZE"], "rxcui": ["1294641", "1740437"], "spl_set_id": ["d8fb000e-3cc9-4803-b71d-2cc597661977"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (67979-002-01) / 1 IMPLANT in 1 VIAL, GLASS", "package_ndc": "67979-002-01", "marketing_start_date": "20070531"}], "brand_name": "SUPPRELIN LA", "product_id": "67979-002_917e915f-4793-48bf-84c3-50272421616f", "dosage_form": "IMPLANT", "pharm_class": ["Gonadotropin Releasing Hormone Receptor Agonist [EPC]", "Gonadotropin Releasing Hormone Receptor Agonists [MoA]"], "product_ndc": "67979-002", "generic_name": "histrelin acetate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUPPRELIN", "brand_name_suffix": "LA", "active_ingredients": [{"name": "HISTRELIN ACETATE", "strength": "50 mg/1"}], "application_number": "NDA022058", "marketing_category": "NDA", "marketing_start_date": "20070531", "listing_expiration_date": "20261231"}