Package 70518-4200-0

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 70518-4200-0
Digits Only 7051842000
Product NDC 70518-4200
Product ID 70518-4200_3ff4e764-1554-cca9-e063-6294a90accb7
Description

10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0)

Marketing

Marketing Status
Marketed Since 2024-10-02
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

Prochlorperazine Maleate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff4e764-1554-cca9-e063-6294a90accb7", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["5c1dd0ea-89e9-4317-a83e-5e15da79ca20"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0)", "package_ndc": "70518-4200-0", "marketing_start_date": "20241002"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70518-4200_3ff4e764-1554-cca9-e063-6294a90accb7", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4200", "generic_name": "Prochlorperazine Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216495", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}