Package 60687-799-17

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 60687-799-17
Digits Only 6068779917
Product NDC 60687-799
Description

10 TRAY in 1 CASE (60687-799-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)

Marketing

Marketing Status
Marketed Since 2024-04-15
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e1c7e24-1a56-569f-e063-6294a90ad540", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["141935"], "spl_set_id": ["862d9bcd-aaaf-4b10-9013-f696f4cf9581"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (60687-799-17)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)", "package_ndc": "60687-799-17", "marketing_start_date": "20240415"}], "brand_name": "Haloperidol", "product_id": "60687-799_2e1c7e24-1a56-569f-e063-6294a90ad540", "dosage_form": "SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "60687-799", "generic_name": "Haloperidol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/mL"}], "application_number": "ANDA073037", "marketing_category": "ANDA", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}