Package 71225-133-02
Brand: dexmedetomidine hydrochloride
Generic: dexmedetomidine hydrochloridePackage Facts
Identity
Package NDC
71225-133-02
Digits Only
7122513302
Product NDC
71225-133
Description
8 BOTTLE in 1 CARTON (71225-133-02) / 100 mL in 1 BOTTLE (71225-133-01)
Marketing
Marketing Status
Brand
dexmedetomidine hydrochloride
Generic
dexmedetomidine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a58fa0dd-e910-4252-9a49-af607fd030ef", "openfda": {"upc": ["0371225133010", "0371225132013"], "unii": ["1018WH7F9I"], "rxcui": ["1718906", "1718909"], "spl_set_id": ["f21d674a-7f5c-4143-82ae-83c43c503084"], "manufacturer_name": ["Slayback Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "8 BOTTLE in 1 CARTON (71225-133-02) / 100 mL in 1 BOTTLE (71225-133-01)", "package_ndc": "71225-133-02", "marketing_start_date": "20211020"}], "brand_name": "DEXMEDETOMIDINE HYDROCHLORIDE", "product_id": "71225-133_a58fa0dd-e910-4252-9a49-af607fd030ef", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha2-Agonists [MoA]", "Central alpha-2 Adrenergic Agonist [EPC]", "General Anesthesia [PE]"], "product_ndc": "71225-133", "generic_name": "dexmedetomidine hydrochloride", "labeler_name": "Slayback Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXMEDETOMIDINE HYDROCHLORIDE", "active_ingredients": [{"name": "DEXMEDETOMIDINE HYDROCHLORIDE", "strength": "4 ug/mL"}], "application_number": "ANDA212791", "marketing_category": "ANDA", "marketing_start_date": "20211020", "listing_expiration_date": "20261231"}