Package 0093-7866-65

Brand: fentanyl citrate

Generic: fentanyl citrate
NDC Package

Package Facts

Identity

Package NDC 0093-7866-65
Digits Only 0093786665
Product NDC 0093-7866
Description

30 BLISTER PACK in 1 CARTON (0093-7866-65) / 1 LOZENGE in 1 BLISTER PACK (0093-7866-19)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand fentanyl citrate
Generic fentanyl citrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL", "TRANSMUCOSAL"], "spl_id": "4dbe9184-14cd-4666-aabf-1b7fece92337", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["310293", "310294", "310295", "310297", "313992", "313993"], "spl_set_id": ["78221eab-66fd-4cd8-9c81-af52eb83671c"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0093-7866-65)  / 1 LOZENGE in 1 BLISTER PACK (0093-7866-19)", "package_ndc": "0093-7866-65", "marketing_end_date": "20260831", "marketing_start_date": "20151208"}], "brand_name": "Fentanyl Citrate", "product_id": "0093-7866_4dbe9184-14cd-4666-aabf-1b7fece92337", "dosage_form": "LOZENGE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0093-7866", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "400 ug/1"}], "application_number": "NDA020747", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260831", "marketing_start_date": "20151208"}