Package 67979-002-01

Brand: supprelin la

Generic: histrelin acetate
NDC Package

Package Facts

Identity

Package NDC 67979-002-01
Digits Only 6797900201
Product NDC 67979-002
Description

1 VIAL, GLASS in 1 CARTON (67979-002-01) / 1 IMPLANT in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2007-05-31
Brand supprelin la
Generic histrelin acetate
Sample Package No

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"}