Package 70518-4498-0

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 70518-4498-0
Digits Only 7051844980
Product NDC 70518-4498
Product ID 70518-4498_41096a22-a36c-964f-e063-6394a90afb9f
Description

20 TABLET in 1 BOTTLE, PLASTIC (70518-4498-0)

Marketing

Marketing Status
Marketed Since 2025-10-11
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41096a22-a36c-964f-e063-6394a90afb9f", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["312635"], "spl_set_id": ["c622550a-4f61-47f7-bc6b-9545d5d4e031"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-4498-0)", "package_ndc": "70518-4498-0", "marketing_start_date": "20251011"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "70518-4498_41096a22-a36c-964f-e063-6394a90afb9f", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4498", "generic_name": "Prochlorperazine Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA217478", "marketing_category": "ANDA", "marketing_start_date": "20251011", "listing_expiration_date": "20261231"}