Package 70518-0035-0

Brand: haloperidol

Generic: haloperidol lactate
NDC Package

Package Facts

Identity

Package NDC 70518-0035-0
Digits Only 7051800350
Product NDC 70518-0035
Product ID 70518-0035_47d237d9-837d-6e8b-e063-6394a90a7493
Description

25 VIAL in 1 TRAY (70518-0035-0) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2016-12-02
Brand haloperidol
Generic haloperidol lactate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "47d237d9-837d-6e8b-e063-6394a90a7493", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["e702b2f0-d464-41c3-977a-d37bb22c0ab0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (70518-0035-0)  / 1 mL in 1 VIAL", "package_ndc": "70518-0035-0", "marketing_start_date": "20161202"}], "brand_name": "Haloperidol", "product_id": "70518-0035_47d237d9-837d-6e8b-e063-6394a90a7493", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70518-0035", "generic_name": "HALOPERIDOL LACTATE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA075689", "marketing_category": "ANDA", "marketing_start_date": "20161202", "listing_expiration_date": "20271231"}