Package 52817-720-05

Brand: apomorphine hydrocloride

Generic: apomorphine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52817-720-05
Digits Only 5281772005
Product NDC 52817-720
Description

5 CARTRIDGE in 1 CARTON (52817-720-05) / 3 mL in 1 CARTRIDGE (52817-720-01)

Marketing

Marketing Status
Marketed Since 2022-02-24
Brand apomorphine hydrocloride
Generic apomorphine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "2fbd7414-f94f-4e18-8d0e-3ae69a5449f7", "openfda": {"unii": ["F39049Y068"], "rxcui": ["855856"], "spl_set_id": ["aedf70e4-1949-44bc-bf1b-0f282c4f0705"], "manufacturer_name": ["TruPharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 CARTRIDGE in 1 CARTON (52817-720-05)  / 3 mL in 1 CARTRIDGE (52817-720-01)", "package_ndc": "52817-720-05", "marketing_start_date": "20220224"}], "brand_name": "apomorphine hydrocloride", "product_id": "52817-720_2fbd7414-f94f-4e18-8d0e-3ae69a5449f7", "dosage_form": "INJECTION", "pharm_class": ["Dopamine Agonists [MoA]", "Dopaminergic Agonist [EPC]"], "product_ndc": "52817-720", "generic_name": "APOMORPHINE HYDROCHLORIDE", "labeler_name": "TruPharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "apomorphine hydrocloride", "active_ingredients": [{"name": "APOMORPHINE HYDROCHLORIDE", "strength": "30 mg/3mL"}], "application_number": "ANDA212025", "marketing_category": "ANDA", "marketing_start_date": "20220224", "listing_expiration_date": "20261231"}