Package 63323-806-50
Brand: fentanyl citrate
Generic: fentanyl citratePackage Facts
Identity
Package NDC
63323-806-50
Digits Only
6332380650
Product NDC
63323-806
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-50) / 50 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
fentanyl citrate
Generic
fentanyl citrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "341b092a-1f6f-40f1-98f2-9346bf2e1242", "openfda": {"upc": ["0363323806132", "0363323806149", "0363323806507"], "unii": ["MUN5LYG46H"], "rxcui": ["1735003", "1735007", "1735008", "1735013", "2168270"], "spl_set_id": ["38d0c14a-a0c1-44cc-a939-0304eb8037d6"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-01) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-806-11)", "package_ndc": "63323-806-01", "marketing_start_date": "20190503"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-02) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-806-12)", "package_ndc": "63323-806-02", "marketing_start_date": "20190503"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-05) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-806-13)", "package_ndc": "63323-806-05", "marketing_start_date": "20190503"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-20) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-806-14)", "package_ndc": "63323-806-20", "marketing_start_date": "20190503"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (63323-806-50) / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "63323-806-50", "marketing_start_date": "20190503"}], "brand_name": "Fentanyl Citrate", "product_id": "63323-806_341b092a-1f6f-40f1-98f2-9346bf2e1242", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63323-806", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": ".05 mg/mL"}], "application_number": "ANDA210762", "marketing_category": "ANDA", "marketing_start_date": "20190503", "listing_expiration_date": "20261231"}