apomorphine hydrocloride

Generic: apomorphine hydrochloride

Labeler: trupharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name apomorphine hydrocloride
Generic Name apomorphine hydrochloride
Labeler trupharma, llc
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

apomorphine hydrochloride 30 mg/3mL

Manufacturer
TruPharma, LLC

Identifiers & Regulatory

Product NDC 52817-720
Product ID 52817-720_2fbd7414-f94f-4e18-8d0e-3ae69a5449f7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212025
Listing Expiration 2026-12-31
Marketing Start 2022-02-24

Pharmacologic Class

Classes
dopamine agonists [moa] dopaminergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817720
Hyphenated Format 52817-720

Supplemental Identifiers

RxCUI
855856
UNII
F39049Y068

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name apomorphine hydrocloride (source: ndc)
Generic Name apomorphine hydrochloride (source: ndc)
Application Number ANDA212025 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/3mL
source: ndc
Packaging
  • 5 CARTRIDGE in 1 CARTON (52817-720-05) / 3 mL in 1 CARTRIDGE (52817-720-01)
source: ndc

Packages (1)

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

Ingredients (1)

apomorphine hydrochloride (30 mg/3mL)

Linked Drug Pages (1)

apomorphine hydrocloride ndc-match (0.9)

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"}